rs16975963
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16975963(C;C) |
Make rs16975963(C;G) |
Make rs16975963(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 37834896 |
Gene | LOC100631378 |
is a | snp |
is | mentioned by |
dbSNP | rs16975963 |
dbSNP (classic) | rs16975963 |
ClinGen | rs16975963 |
ebi | rs16975963 |
HLI | rs16975963 |
Exac | rs16975963 |
Gnomad | rs16975963 |
Varsome | rs16975963 |
LitVar | rs16975963 |
Map | rs16975963 |
PheGenI | rs16975963 |
Biobank | rs16975963 |
1000 genomes | rs16975963 |
hgdp | rs16975963 |
ensembl | rs16975963 |
geneview | rs16975963 |
scholar | rs16975963 |
rs16975963 | |
pharmgkb | rs16975963 |
gwascentral | rs16975963 |
openSNP | rs16975963 |
23andMe | rs16975963 |
SNPshot | rs16975963 |
SNPdbe | rs16975963 |
MSV3d | rs16975963 |
GWAS Ctlg | rs16975963 |
GMAF | 0.2557 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20834067] |
Trait | |
Title | Joint influence of small-effect genetic variants on human longevity. |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | None None |