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rs2516739

From SNPedia

Orientationminus
Stabilizedminus
Make rs2516739(C;C)
Make rs2516739(C;T)
Make rs2516739(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position2047157
GeneNTHL1, TSC2
is asnp
is mentioned by
dbSNPrs2516739
ebirs2516739
HLIrs2516739
Exacrs2516739
Varsomers2516739
Maprs2516739
PheGenIrs2516739
hapmaprs2516739
1000 genomesrs2516739
hgdprs2516739
ensemblrs2516739
gopubmedrs2516739
geneviewrs2516739
scholarrs2516739
googlers2516739
pharmgkbrs2516739
gwascentralrs2516739
openSNPrs2516739
23andMers2516739
23andMe allrs2516739
SNP Nexus

SNPshotrs2516739
SNPdbers2516739
MSV3drs2516739
GWAS Ctlgrs2516739
GMAF0.2452
Max Magnitude
? (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