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rs9786640

From SNPedia

Orientationplus
Stabilizedplus
Make rs9786640(A;A)
Make rs9786640(A;C)
Make rs9786640(C;C)
ReferenceGRCh38 38.1/141
ChromosomeY
Position12527496
is asnp
is mentioned by
dbSNPrs9786640
ebirs9786640
HLIrs9786640
Exacrs9786640
Varsomers9786640
Maprs9786640
PheGenIrs9786640
hapmaprs9786640
1000 genomesrs9786640
hgdprs9786640
ensemblrs9786640
gopubmedrs9786640
geneviewrs9786640
scholarrs9786640
googlers9786640
pharmgkbrs9786640
gwascentralrs9786640
openSNPrs9786640
23andMers9786640
23andMe allrs9786640
SNP Nexus

SNPshotrs9786640
SNPdbers9786640
MSV3drs9786640
GWAS Ctlgrs9786640
Y Chromrs9786640
Max Magnitude

[PMID 19495413OA-icon.png] Improved resolution haplogroup G phylogeny in the Y chromosome, revealed by a set of newly characterized SNPs.