$88.00

J1-BY8 Panel
[BY8Panel]

J1-BY8 Panel
This is a 2 round panel that pinpoints the terminal SNP below J1-BY8. This panel is suggested when you have tested BY8+ or if you have a clear prediction for this haplogroup according to your Y-STR results.

In the first round 2 important SNPs will be tested to find out the main category:

BY9
FGC19909

Then we work down the branches iteratively until we have found your position on the given tree.

The test is completed when the unique phylogenetic position on the tree has been determined.

See this tree diagram to understand the groupings in this panel:



Branches covered by this panel:
BY8, ZS4062, BY186550, BY187366, Y163160, BY13768, ZS4063, BY14436, Y21752, BY35549, BY14444, BY4060, Y22085, BY160050, FT167804, Y211479, Y21751, Y60104, Y92836, Y142009, BY4061, FT151489, ZS9187, Y153053, BY162866, BY9, FT264050, ZS12612, FT220561, FGC58290, BY103640, Y133592, Y133665, FGC58306, FGC58317, FGC58302, PH282, BY67220, Y14418, Y14419, HU191, ZS6043, ZS6053, ZS6044, ZS6039, ZS6038, ZS8265, ZS11462, ZS11468, ZS10261, ZS10262, ZS10267, ZS10269, Y14282, BY60366, PR4849, Y13964, Y141956, ZS6861, FGC14302, FT388822, A24115, Y30965, Y137038, BY131225, FT19488, FT391598, ZS7684, FT70844, FGC14310, FT14572, Z42543, ZS12352, FT37427, FT36831, ZS12372, BY118748, FGC19909, BY14465, BY14463, ZS6453, BY180670, ZS6448, ZS6454, ZS6707, ZS6713, BY205807, Y13399, FGC64473, FGC64477, BY110771, Y21760, BY202968, ZS5637, Y85066, FGC58487, ZS1986, FGC58488, ZS5486, FGC58489, ZS12577, FGC29860, FGC29863, FGC31322, Y133594, ZS2030, BY25883, ZS2036, ZS2033, ZS2031, Y94834, ALK521, ZS4242, Y134509, Y134508, Y167261, Y139865, Y187624, ZS4226, FT154965, FT153408, FT154749, FT397047, FT397043, A26337, FGC78668, Y49884, ZS2017, FT83824, BY159229, BY200998, FT131748, FGC19901, ZS10047, Y85275, Y91773, ZS10044, FGC67346, FT4541, FGC67338, BY182880, FT156772, Z39629, ZS2010, FT407412, ZS9515, ZS2007, FGC67322, BY177896, FT8592, FT9766, BY83264, BY175814, FGC19906, Y162269, Y162379

YSEQ reserves the right to replace not working SNPs against phylo-equivalent alternatives if necessary.

Last update 2021-06-24

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