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rs6569992

From SNPedia

Orientationplus
Stabilizedplus
Make rs6569992(A;A)
Make rs6569992(A;G)
Make rs6569992(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position135131014
is asnp
is mentioned by
dbSNPrs6569992
ebirs6569992
HLIrs6569992
Exacrs6569992
Varsomers6569992
Maprs6569992
PheGenIrs6569992
hapmaprs6569992
1000 genomesrs6569992
hgdprs6569992
ensemblrs6569992
gopubmedrs6569992
geneviewrs6569992
scholarrs6569992
googlers6569992
pharmgkbrs6569992
gwascentralrs6569992
openSNPrs6569992
23andMers6569992
23andMe allrs6569992
SNP Nexus

SNPshotrs6569992
SNPdbers6569992
MSV3drs6569992
GWAS Ctlgrs6569992
GMAF0.1873
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20927387OA-icon.png]
Trait
Title A genome-wide association study of red blood cell traits using the electronic medical record
Risk Allele A
P-val 3E-8
Odds Ratio 0.75 [0.48-1.02] unit increase