Rs17250992

From SNPedia
Jump to: navigation, search

Orientationplus
Geno Mag Summary
(T;T) Relevant to haplogroup P
Make rs17250992(C;C)
Make rs17250992(C;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position8977339
is asnp
is mentioned by
dbSNPrs17250992
Exacrs17250992
PheGenIrs17250992
nextbiors17250992
hapmaprs17250992
1000 genomesrs17250992
hgdprs17250992
ensemblrs17250992
gopubmedrs17250992
geneviewrs17250992
scholarrs17250992
googlers17250992
pharmgkbrs17250992
gwascentralrs17250992
openSNPrs17250992
23andMers17250992
23andMe allrs17250992
SNP Nexus

SNPshotrs17250992
SNPdbers17250992
MSV3drs17250992
Y Chromrs17250992
Max Magnitude
[PMID 18385274] This snp distinguishes haplogroups