rs2031577
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2031577(C;C) |
Make rs2031577(C;T) |
Make rs2031577(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 4007811 |
is a | snp |
is | mentioned by |
dbSNP | rs2031577 |
dbSNP (classic) | rs2031577 |
ClinGen | rs2031577 |
ebi | rs2031577 |
HLI | rs2031577 |
Exac | rs2031577 |
Gnomad | rs2031577 |
Varsome | rs2031577 |
LitVar | rs2031577 |
Map | rs2031577 |
PheGenI | rs2031577 |
Biobank | rs2031577 |
1000 genomes | rs2031577 |
hgdp | rs2031577 |
ensembl | rs2031577 |
geneview | rs2031577 |
scholar | rs2031577 |
rs2031577 | |
pharmgkb | rs2031577 |
gwascentral | rs2031577 |
openSNP | rs2031577 |
23andMe | rs2031577 |
SNPshot | rs2031577 |
SNPdbe | rs2031577 |
MSV3d | rs2031577 |
GWAS Ctlg | rs2031577 |
GMAF | 0.4403 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 |