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rs2031577

From SNPedia

Orientationminus
Stabilizedminus
Make rs2031577(C;C)
Make rs2031577(C;T)
Make rs2031577(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position4007811
is asnp
is mentioned by
dbSNPrs2031577
dbSNP (classic)rs2031577
ClinGenrs2031577
ebirs2031577
HLIrs2031577
Exacrs2031577
Gnomadrs2031577
Varsomers2031577
LitVarrs2031577
Maprs2031577
PheGenIrs2031577
Biobankrs2031577
1000 genomesrs2031577
hgdprs2031577
ensemblrs2031577
geneviewrs2031577
scholarrs2031577
googlers2031577
pharmgkbrs2031577
gwascentralrs2031577
openSNPrs2031577
23andMers2031577
SNPshotrs2031577
SNPdbers2031577
MSV3drs2031577
GWAS Ctlgrs2031577
GMAF0.4403
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 20834067OA-icon.png]
Trait
Title Joint influence of small-effect genetic variants on human longevity.
Risk Allele
P-val 0.000001
Odds Ratio None None