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rs9786608

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) Relevant to haplogroup E
Make rs9786608(C;C)
Make rs9786608(C;T)
Make rs9786608(T;T)
ReferenceGRCh38 38.1/141
ChromosomeY
Position2795902
is asnp
is mentioned by
dbSNPrs9786608
ebirs9786608
HLIrs9786608
Exacrs9786608
Varsomers9786608
Maprs9786608
PheGenIrs9786608
hapmaprs9786608
1000 genomesrs9786608
hgdprs9786608
ensemblrs9786608
gopubmedrs9786608
geneviewrs9786608
scholarrs9786608
googlers9786608
pharmgkbrs9786608
gwascentralrs9786608
openSNPrs9786608
23andMers9786608
23andMe allrs9786608
SNP Nexus

SNPshotrs9786608
SNPdbers9786608
MSV3drs9786608
GWAS Ctlgrs9786608
Y Chromrs9786608
GMAF0.2204
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 18385274] This snp distinguishes haplogroups