Y-DNA (37 markers) database
including Rurikid princes and those males who are also suspecting their descent
from Rurik (the 1st Russian prince, 9th century).
Contains currently the following surnames : Gagarin, Gorchakov, Kosonen,
Lobanov-Rostovsky, Mozarowski (and variants), Mozhaysky, Niewmierzycki (and
variants), Obolensky, Ossowiecki, Poscharsky, Puzyna, Rostowsky, Rzhevsky,
Shahovskoi, Solomin, Szuyski, Tolloczko and Volkonsky. However, in spite of
their “princely” surnames, only a couple of them were found to be genetic
descendants of Rurik. Besides, it was discovered that the Volkonsky/Obolensky
branch is of Slavic descent (genetic haplogroup R1a1), and most probably the
princes in this branch are not descended from Rurik. By all means it seems that
Rurik was a historical person who was born on the Roslagen seashore (slightly
north of Stockholm, Sweden). However, he was of the Finno-Ugrian descent
(haplogroup N1c1 (earlier described as N3a) -
although, theoretically, this could have been the Obolensky branch which
might be descended from Rurik). The prince Piotr Szuyski is also of Slavic
descent (R1a1). It seems that this was the prince St. Yaroslav Vsevolodovich
(b. 1191), who wasn’t genetic son of the prince Vsevolod Yurievich “Bolshoe
Gnezdo” (The Big Nest).
Since the two branches, i.e. the
Chernigov-Kievan (Volkonsky, Obolensky) and the Muscovite (Szuysky) are somehow
related by blood, it seems that two different members of the same ruling
dynasty broke these lines. Myself, I think that the Chernigov branch was broken
by the king Boleslaw II Smialy (either in the year 1069 or in the years
1077/78), while the Muscovite branch was broken by Mikolaj Lis, the voievod in
Krakow (Cracow), the then capital of Poland. Lis left Ukraine in may 1190. 9
months later St. Jaroslav Vsevolodovich was born. According to some Polish
genealogists the Lis clan might be originated from the Polish ruling Piast
dynasty.
Results for people whose surnames
are marked with green background were provided by Nikita Maximov, the
Scientific Editor of the Russian Newsweek Magazine. They are not to be taken
away from here unless a written permission from him will be obtained (nmaximov@gmail.com) .
Other results are freely available
to anyone who wishes to use them for comparative and non-commercial purposes.
However, neither test result can be taken away from here by a male (nor by his
closest relative) who made his own Y-DNA test, but himself doesn’t wish to
inform the public of his result.
Mutation rates in markers marked with
pink background are larger (0.003 to 0.005), and those marked with violet background are extremely large (above
0.005) compared with an average mutation
rate (which is something like 0.0024). However, in the so-called genetic
calculator one can also use different mutation rates in each of the marker
panels. Estimated more precisely by the FTDNA Co., the average mutation rates
are as follows : 0.00399 (markers 1 – 12), 0.00481 (markers 13 – 25), and
0.00748 (markers 26 - 37), respectively (http://www.mymcgee.com/tools/yutility.html#MutationRate)
. And this is also a clear evidence for this that the markers 26 – 37 are most
important in genetic genealogy. When comparing the markers 1 –25 one can only
SUSPECT that the two tested males might be related by blood if their markers
are matching. By ALL MEANS one needs to check the markers 26 – 37, and
especially the fast mutating markers like CDYa, CDYb and DYS 570, to be
absolutely CERTAIN that, IN FACT, he IS related by blood with another man. A
lot of Y-DNA test results do appear on the Y-search.org database (http://www.ysearch.org/) when the two males
are e.g. perfectly matching on their first 12 markers; a certain mismatch,
however, small, can appear on the 2nd panel (markers 13 - 25); while
a considerable mismatch on the 3rd panel (markers 26 – 37) is a
clear evidence for this that they have not been related by blood at all (in
historical times – 50-60 generations ago).
Thanks to this project I can verify
real mutation rates, and these have been displayed below. The rates are
calculated per the entire 37 markers haplotypes and per century. The time that
passed by is a difference between the year in which the Y-DNA tests were
performed, and the year when the common male ancestor (CMA) was born.
Surname andgiven
name |
Surname andgiven
name |
Haplogroup |
Common maleancestor (CMA) |
Year born |
Centuries tothe
CMA |
Genetic Distance |
Mutation rate per 37 markers haplotype and per century**
|
||
|
(in blue SNP test) |
FTDNA
standard* |
Webmaster’s
standard* |
FTDNA
standard* |
Webmaster’s
standard* |
|||||
Belikov1
(Belevsky) |
RzhevskyNikolai |
N1c1
|
YaroslavThe Wise |
978 |
10.30 |
12 |
9 |
1.1650 |
0.8738 |
Gagarin
G.G. |
RzhevskyNikolai |
N1c1
|
Vladimir
Monomakh |
1053 |
9.55 |
3@ |
3@ |
0.4649@ |
0.4649@ |
Gagarin
A.P. |
RzhevskyNikolai |
N1c1
|
VladimirMonomakh |
1053 |
9.55 |
4 |
4 |
0.4188 |
0.4188 |
KhovanskiiAskold |
ChartoriskyAlex |
N1c1
|
Gedimin
|
Ab. 1270 |
7.38 |
4 |
4 |
0.5420 |
0.5420 |
TAWAST
|
CLAN
|
(***; 4)
|
AVERAGE
|
|
|
|
|
0.4645 |
0.3787 |
TawastHannu |
StjernaAntti |
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
4 |
3 |
0.7874 |
0.5906 |
Tawast
Hannu |
TawastVeikko |
N1c1
|
Tawast
Christoffer |
Ab.
1660 |
3.47 |
2@@ |
2@@ |
0.5764@@ |
0.5764@@ |
TawastHannu |
TawastJ. |
N1c1
|
Tawast
Christoffer |
Ab.
1660 |
3.47 |
3 |
3 |
0.8646 |
0.8646 |
TawastHannu |
TawastT. |
N1c1
|
Tawast
Alexander |
1802 |
2.07 |
1@@ |
1@@ |
0.4831@@ |
0.4831@@ |
Tawast
Hannu
|
Bergh
P.
|
N1c1
|
Tawast
Johan |
Ab.
1590 |
4.17 |
2 |
2 |
0.4796 |
0.4796 |
Stjerna
Antti
|
Tawast
Veikko |
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
2 |
1 |
0.3937 |
0.1969 |
Stjerna
Antti
|
Tawast
J. |
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
3 |
2 |
0.5906 |
0.3937 |
Stjerna
Antti
|
Tawast
T. |
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
3 |
2 |
0.5906 |
0.3937 |
Stjerna
Antti
|
Bergh
P. |
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
2 |
1 |
0.3937 |
0.1969 |
TawastVeikko |
TawastJ. |
N1c1
|
TawastFrederik |
1758 |
2.50 |
1 |
1 |
0.4000 |
0.4000 |
Tawast
Veikko
|
Tawast
T.
|
N1c1
|
Tawast
Christoffer |
Ab.
1660 |
3.47 |
1 |
1 |
0.2882 |
0.2882 |
Tawast
Veikko.
|
Bergh
P.
|
N1c1
|
TawastJohan |
Ab.
1590 |
4.17 |
0 |
0 |
0 |
0 |
TawastT.
|
Tawast
J.
|
N1c1
|
TawastChristoffer |
Ab.
1660 |
3.47 |
2 |
2 |
0.5764 |
0.5764 |
Tawast
T.
|
Bergh
P.
|
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
1 |
1 |
0.1969 |
0.1969 |
Tawast
J.
|
Bergh
P.
|
N1c1
|
Tawast
Henrik |
Ab.
1500 |
5.08 |
1 |
1 |
0.1969 |
0.1969 |
|
|
|
|
|
|
|
|
|
|
|
Vines
Fred |
VinesRon |
N1c1 |
VinesJohn |
Ab. 1660 |
3.46 |
2@@ |
2@@ |
0.5764@@ |
0.5764@@ |
VinesFred |
VinesPaul B. |
N1c1 |
VinesEdward |
1725 |
2.81 |
1@ |
1@ |
0.5267@ |
0.5267@ |
Kosonen
Roy |
Kosonen
Eino |
N1c1
|
Kosoin
Petteri |
1713 |
2.94 |
1 |
1 |
0.3436 |
0.3436 |
FletcherBrien |
FletcherRichard |
N1c1 |
FletcherJohn
S. |
1829 |
1.79 |
3 |
2 |
1.6760 |
1.1173 |
Lapinski
“Wzorek” |
Lapinski
„Bodaj” |
R1a12
|
Lapinski
Jakub |
Ab. 1510 |
4.98 |
4 |
4 |
0.8032 |
0.8032 |
Lapinski
„Kus” |
Lapinski
„Bodaj” |
R1a1
|
Lapinski
Wit |
Ab. 1450 |
5.58 |
5 |
5 |
0.8961 |
0.8961 |
Lapinski
„Rosman” |
Lapinski
„Bodaj” |
R1a1
|
Lapinski
„Lapa” |
Ab. 1420 |
5.88 |
4 |
4 |
0.6803 |
0.6803 |
Lapinski
„Wzorek” |
Lapinski
„Kus” |
R1a1
|
Lapinski
Wit |
Ab. 1450 |
5.58 |
5 |
5 |
0.8961 |
0.8961 |
Lapinski
„Rosman” |
Lapinski
„Kus” |
R1a1
|
Lapinski
„Lapa” |
Ab. 1420 |
5.88 |
3 |
3 |
0.5102 |
0.5102 |
Lapinski
„Rosman” |
Lapinski
„Wzorek“ |
R1a1
|
Lapinski
„Lapa” |
Ab. 1420 |
5.88 |
6 |
6 |
1.0204 |
1.0204 |
Kossacki-
Lytwyn Lukasz |
Kossacki-
Lytwyn Jacek
|
R1a1
|
|
1900 |
1.08 |
2 |
2 |
1.8519 |
1.8519 |
Plewako
Stanislaw J. |
Plewako
Stanislaw G. |
I2a3
|
Plewako
Kazimierz |
1822 |
1.87 |
1 |
1 |
0.5348@@ |
0.5348@@ |
·
* In almost 100 % of all cases, unexpectedly, some of
the markers AMONG THE FINNs (N1c1) seem to be MUTATING SIMULTANEOUSLY (or very
shortly one after another). This observation is valid in the case of the
following pairs of markers : DYS 459 a and DYS 459 b, DYS 464 a and DYS 464 b,
DYS 464 c and DYS 464 d, as well as CDY a and CDY b. The FTDNA Co. is not
taking this phenomenon into account at all. For example, if two males are
having 37 37 and 34 34 in CDY a and CDY b, respectively, the FTDNA Co. counts
the genetic distance (GD) to be 3x2=6 in the both markers. I will try to
reconsider this problem, and in the right column the GD = 3 in such case will
be counted. The future will show which method is correct.
·
** To compare these figures with those mentioned above,
one needs to divide them by 37x4 (4 generations per century), i.e. by 148.
·
@25 markers, i.e. only markers 1-25 are compared.
However, in this case the result of simple division is multiplied by 37/25 to
arrive at figures adequate for 37 markers tests.
·
@@The same result has been obtained for the 67 markers
haplotype.
·
*** Average mutation rate is calculated only for those
clans which can deliver at least 10 documented results. This average is
calculated in the following way : 20 % of minimal, as well as 20 % of maximal
results, are being discarded; the average is being calculated from the
remaining 60 % of all the results among the clan.
·
1 Mr. Belikov’s family was living in Belarus (earlier
in the Grand Duchy of Lithuania). Mr. Belikov by all means is a genetic Rurikid.
It’s almost certain that his family originated from the Belevsky princes. Two
Belevskys in 15th century settled themselves in the Gr. Duchy of
Lithuania.
·
2 By courtesy of
Lukasz Lubicz-Lapinski and his Lapinski Clan Y-DNA project (lapinski_szla@wp.pl; http://www.familytreedna.com/public/Lapinski)
·
3 By courtesy of
Stanislaw J. Plewako (http://www.familytreedna.com/public/Plewako/default.aspx?section=yresults)
·
4 By courtesy of Hannu Tawast (hannu.tawast@pp.inet.fi)
Genetic distance |
-6 |
-5 |
-4 |
-3 |
-2 |
-1 |
0 (Perfect match) |
+1 |
+2 |
+3 |
+4 |
+5 |
+6 |
Background |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Column Raw |
|
|
|
|
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
13 |
14 |
15 |
16 |
17 |
18 |
19 |
20 |
21 |
22 |
23 |
24 |
25 |
26 |
27 |
28 |
29 |
30 |
31 |
32 |
33 |
34 |
35 |
36 |
37 |
Markers
non matching either those of the mo- dal
Rurikid (green) or |
Remarks |
TMRCA 3/ and/or additional remarks |
|
Surname
and (the 1st) given
name (FINNISH MONOMAKH BRANCH) |
Number displayed
here with coloured background indicates a kinship |
Father’s given name |
Date of
birth |
Place of
birth |
Haplo- group (in blue determi- ned by SNP test) |
D Y S 3 9 3 |
D Y S 3 9 0 |
D Y S 19/ 3 9 4 |
D Y S 3 9 1 |
D Y S 3 8 5 a |
D Y S 3 8 5 b |
D Y S 4 2 6 |
D Y S 3 8 8 |
D Y S 4 3 9 |
D Y S 3 8 9 _1 |
D Y S 3 9 2 |
D Y S 3 8 9 _2 |
D Y S 4 5 8 |
D Y S 4 5 9 a |
D Y S 4 5 9 b |
D Y S 4 5 5 |
D Y S 4 5 4 |
D Y S 4 4 7 |
D Y S 4 3 7 |
D Y S 4 4 8 |
D Y S 4 4 9 |
D Y S 4 6 4 a |
D Y S 4 6 4 b |
D Y S 4 6 4 c |
D Y S 4 6 4 d |
D Y S 4 6 0 |
G A T A H 4 |
Y C A II a |
Y C A II b |
D Y S 4 5 6 |
D Y S 6 0 7 |
D Y S 5 7 6 |
D Y S 5 7 0 |
C D Y a |
C D Y b |
D Y S 4 4 2 |
D Y S 4 3 8 |
Woroniecki (violet)
or Trubetsky
(pink) or Mozarowski (yellow
field), respectively |
|
|
|
|
Modal Haplotype N2-A1 |
Pink background in this |
|
Pink background in this |
(^) |
13 |
23 |
14 |
10 |
12 |
13 |
|
|
10 |
13 |
14 |
30 |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
10 |
|
|
|
|
|
Modal Haplotype N2-A2 |
column indicates a person |
|
column indicates a person |
(^) |
13 |
23 |
15 |
11 |
12 |
13 |
|
|
11 |
13 |
14 |
30 |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
11 |
|
|
|
|
|
Modal Haplotype N3a
(N1c1) |
whose princely descent
is |
|
whose princely descent
is |
(^) |
14 |
23 |
14 |
11 |
11 |
13 |
|
|
10 |
14 |
14 |
30 |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
10 |
|
|
|
|
|
Modal Haplotype N3a2 |
proved with documents |
|
confirmed by family tradition |
(^) |
14 |
23 |
14 |
10 |
11 |
13 |
|
|
10 |
14 |
14 |
30 |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
10 |
|
|
|
|
Rurik
the 1st
Russian Prince
(**) |
Modal Haplotype |
Unknown (**) |
Ca. 820 |
Uppland Province Sweden |
(N1c1) (**) |
14 |
23 |
14 |
11 |
11 |
13 |
11 |
12 |
10 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
12 |
25 |
14 |
19 |
29 |
14 |
14 |
15 |
15 |
11 |
11 |
18 |
20 |
14 |
15 |
16 |
19 |
35 |
35 |
14 |
10 |
|
|
|
|
Rzhevsky Nikolai |
1 Rurikid Smolensk branch |
(+) |
|
|
N1c1
|
14 |
23 |
14 |
11 |
11 |
13 |
11 |
12 |
10 |
14 |
14 |
31 |
18 |
9 |
9 |
10 |
12 |
25 |
14 |
19 |
29 |
14 |
14 |
15 |
15 |
12 |
11 |
18 |
20 |
14 |
15 |
16 |
19 |
34 |
34 |
14 |
10 |
5
(genetic distance = 4) |
Genetically
he is an Ugro-Finn |
|
|
Shahovskoi Dmitri |
2 Rurikid Yaroslavl branch |
Mikhail |
1934 |
France |
N1c1 |
14 |
23 |
14 |
11 |
11 |
13 |
|
|
10 |
14 |
14 |
31 |
|
|
|
|
|
|
14 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
10 |
1
(genetic distance = 1) |
Genetically
he is an Ugro-Finn |
|
|
Gagarin Grigori |
3 Rurikid Starodub branch |
Grigori |
|
|
N1c1 |
14 |
23 |
14 |
11 |
11 |
13 |
11 |
12 |
10 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
12 |
25 |
14 |
19 |
29 |
14 |
14 |
15 |
15 |
|
|
|
|
|
|
|
|
|
|
|
|
0
(genetic distance = 0) |
Genetically
he is an Ugro-Finn |
|
|
Gagarin Andrei |
3a
Rurikid Starodub branch |
Petr |
1935 |
|
N1c1
|
14 |
23 |
14 |
11 |
11 |
13 |
11 |
12 |
10 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
12 |
25 |
14 |
19 |
29 |
14 |
15 |
15 |
15 |
12 |
11 |
18 |
20 |
14 |
15 |
16 |
18 |
34 |
34 |
14 |
10 |
5
(genetic distance = 4) |
Genetically
he is an Ugro-Finn |
|
|
Lobanov- Rostovsky Nikita |
4 Rurikid Rostov branch |
Dmitry |
6 JAN 1935 |
Sophia Bulgaria |
N1c1 |
14 |
23 |
|
11 |
12 |
13 |
|
|
10 |
14 |
14 |
30 |
|
|
|
|
|
|
14 |
19 |
|
|
|
|
|
|
12 |
|
|
14 |
|
|
|
|
|
|
10 |
2
(genetic distance = 2) |
Genetically
he is an Ugro-Finn |
|
|
Korsstrom Stefan (*) |
5 Rurikid Unknown branch |
(***) |
|
|
N1c1 |
14 |
23 |
14 |
11 |
11 |
13 |
11 |
12 |
10 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
12 |
25 |
14 |
19 |
28 |
14 |
14 |
15 |
15 |
10 |
10 |
18 |
20 |
14 |
15 |
16 |
19 |
34 |
34 |
15 |
10 |
6
(genetic distance = 5) |
Genetically
he is an Ugro-Finn |
|
|
Nagle Gordon C. |
5aRurikid Unknown branch |
|
|
|
N1c1 |
14 |
23 |
15 |
11 |
11 |
13 |
11 |
13 |
10 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
12 |
24 |
15 |
19 |
28 |
14 |
14 |
15 |
15 |
11 |
11 |
19 |
20 |
14 |
15 |
16 |
19 |
34 |
34 |
14 |
10 |
8
(genetic distance = 7) |
Genetically
he is an Ugro-Finn |
|
|
Lawrence David |
6 Rurikid Unknown branch |
(****) |
|
England |
N1c1
|
14 |
23 |
14 |
11 |
12 |
14 |
11 |
12 |
10 |
15 |
14 |
31 |
18 |
9 |
9 |
11 |
12 |
25 |
14 |
19 |
28 |
14 |
14 |
15 |
15 |
11 |
11 |
18 |
20 |
14 |
15 |
16 |
19 |
35 |
35 |
14 |
10 |
5
(genetic distance = 4) |
Genetically
he is an Ugro-Finn |
|
|
Roundsley (Piotrowski ?) David (*) |
7 Rurikid Unknown branch |
(****) |
|
|
N1c1 |
14 |
23 |
14 |
11 |
13 |
13 |
11 |
12 |
11 |
14 |
14 |
30 |
18 |
9 |
9 |
11 |
15 |
25 |
14 |
19 |
28 |
14 |
14 |
15 |
15 |
11 |
11 |
19 |
20 |
14 |
15 |
16 |
19 |
35 |
35 |
14 |
10 |
5
(genetic distance = 6) |
Genetically
he is an Ugro-Finn |
|
|
Palomaki Esko (#) (*) |
7a
Rurikid Unknown branch |
(****) |
|
|
N1c1 |
14 |
23 |
14 |
11 |
13 |