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rs1698064

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) Relevant to haplogroup NO
Make rs1698064(C;C)
Make rs1698064(C;T)
Make rs1698064(T;T)
ReferenceGRCh38 38.1/141
Chromosome21
Position31783294
is asnp
is mentioned by
dbSNPrs1698064
ebirs1698064
HLIrs1698064
Exacrs1698064
Varsomers1698064
Maprs1698064
PheGenIrs1698064
hapmaprs1698064
1000 genomesrs1698064
hgdprs1698064
ensemblrs1698064
gopubmedrs1698064
geneviewrs1698064
scholarrs1698064
googlers1698064
pharmgkbrs1698064
gwascentralrs1698064
openSNPrs1698064
23andMers1698064
23andMe allrs1698064
SNP Nexus

SNPshotrs1698064
SNPdbers1698064
MSV3drs1698064
GWAS Ctlgrs1698064
GMAF0.4458
Max Magnitude
[PMID 18385274] This snp distinguishes haplogroups