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rs7567389

From SNPedia

Orientationplus
Stabilizedplus
Make rs7567389(A;A)
Make rs7567389(A;T)
Make rs7567389(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position127225069
is asnp
is mentioned by
dbSNPrs7567389
ebirs7567389
HLIrs7567389
Exacrs7567389
Varsomers7567389
Maprs7567389
PheGenIrs7567389
hapmaprs7567389
1000 genomesrs7567389
hgdprs7567389
ensemblrs7567389
gopubmedrs7567389
geneviewrs7567389
scholarrs7567389
googlers7567389
pharmgkbrs7567389
gwascentralrs7567389
openSNPrs7567389
23andMers7567389
23andMe allrs7567389
SNP Nexus

SNPshotrs7567389
SNPdbers7567389
MSV3drs7567389
GWAS Ctlgrs7567389
GMAF0.2475
Max Magnitude
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 20707712OA-icon.png]
Trait
Title A genome-wide association study of self-rated health
Risk Allele A
P-val 0.000002
Odds Ratio 0.03 [NR] unit decrease