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rs9257691

From SNPedia

Orientationplus
Stabilizedplus
Make rs9257691(A;A)
Make rs9257691(A;C)
Make rs9257691(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position29301152
is asnp
is mentioned by
dbSNPrs9257691
ebirs9257691
HLIrs9257691
Exacrs9257691
Varsomers9257691
Maprs9257691
PheGenIrs9257691
hapmaprs9257691
1000 genomesrs9257691
hgdprs9257691
ensemblrs9257691
gopubmedrs9257691
geneviewrs9257691
scholarrs9257691
googlers9257691
pharmgkbrs9257691
gwascentralrs9257691
openSNPrs9257691
23andMers9257691
23andMe allrs9257691
SNP Nexus

SNPshotrs9257691
SNPdbers9257691
MSV3drs9257691
GWAS Ctlgrs9257691
GMAF0.3742
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 22579560] Haplotype specific alteration of diabetes mhc risk by olfactory receptor gene polymorphism