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rs16975963

From SNPedia

Orientationplus
Stabilizedplus
Make rs16975963(C;C)
Make rs16975963(C;G)
Make rs16975963(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position37834896
GeneLOC100631378
is asnp
is mentioned by
dbSNPrs16975963
dbSNP (classic)rs16975963
ClinGenrs16975963
ebirs16975963
HLIrs16975963
Exacrs16975963
Gnomadrs16975963
Varsomers16975963
LitVarrs16975963
Maprs16975963
PheGenIrs16975963
Biobankrs16975963
1000 genomesrs16975963
hgdprs16975963
ensemblrs16975963
geneviewrs16975963
scholarrs16975963
googlers16975963
pharmgkbrs16975963
gwascentralrs16975963
openSNPrs16975963
23andMers16975963
SNPshotrs16975963
SNPdbers16975963
MSV3drs16975963
GWAS Ctlgrs16975963
GMAF0.2557
Max Magnitude0
? (C;C) (C;G) (G;G) 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