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rs3916164

From SNPedia

Orientationplus
Stabilizedplus
Make rs3916164(A;A)
Make rs3916164(A;G)
Make rs3916164(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position39604267
is asnp
is mentioned by
dbSNPrs3916164
ebirs3916164
HLIrs3916164
Exacrs3916164
Varsomers3916164
Maprs3916164
PheGenIrs3916164
hapmaprs3916164
1000 genomesrs3916164
hgdprs3916164
ensemblrs3916164
gopubmedrs3916164
geneviewrs3916164
scholarrs3916164
googlers3916164
pharmgkbrs3916164
gwascentralrs3916164
openSNPrs3916164
23andMers3916164
23andMe allrs3916164
SNP Nexus

SNPshotrs3916164
SNPdbers3916164
MSV3drs3916164
GWAS Ctlgrs3916164
GMAF0.1827
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23222517OA-icon.png]
Trait Red blood cell traits
Title Seventy-five genetic loci influencing the human red blood cell.
Risk Allele G
P-val 3E-10
Odds Ratio .01 [0.0072-0.0088] unit increase