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rs917692

From SNPedia

Orientationminus
Stabilizedminus
Make rs917692(C;C)
Make rs917692(C;T)
Make rs917692(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position28326032
is asnp
is mentioned by
dbSNPrs917692
ebirs917692
HLIrs917692
Exacrs917692
Varsomers917692
Maprs917692
PheGenIrs917692
hapmaprs917692
1000 genomesrs917692
hgdprs917692
ensemblrs917692
gopubmedrs917692
geneviewrs917692
scholarrs917692
googlers917692
pharmgkbrs917692
gwascentralrs917692
openSNPrs917692
23andMers917692
23andMe allrs917692
SNP Nexus

SNPshotrs917692
SNPdbers917692
MSV3drs917692
GWAS Ctlgrs917692
Merged fromRs12964873
Max Magnitude
? (C;C) (C;T) (T;T) 28