rs8001976
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs8001976(C;C) |
Make rs8001976(C;T) |
Make rs8001976(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 47813587 |
is a | snp |
is | mentioned by |
dbSNP | rs8001976 |
dbSNP (classic) | rs8001976 |
ClinGen | rs8001976 |
ebi | rs8001976 |
HLI | rs8001976 |
Exac | rs8001976 |
Gnomad | rs8001976 |
Varsome | rs8001976 |
LitVar | rs8001976 |
Map | rs8001976 |
PheGenI | rs8001976 |
Biobank | rs8001976 |
1000 genomes | rs8001976 |
hgdp | rs8001976 |
ensembl | rs8001976 |
geneview | rs8001976 |
scholar | rs8001976 |
rs8001976 | |
pharmgkb | rs8001976 |
gwascentral | rs8001976 |
openSNP | rs8001976 |
23andMe | rs8001976 |
SNPshot | rs8001976 |
SNPdbe | rs8001976 |
MSV3d | rs8001976 |
GWAS Ctlg | rs8001976 |
GMAF | 0.4371 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21782286] |
Trait | |
Title | A genome-wide association study of aging. |
Risk Allele | T |
P-val | 0.000003 |
Odds Ratio | 1.0900 [NR] |