rs6813479
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6813479(A;A) |
Make rs6813479(A;T) |
Make rs6813479(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 136739228 |
is a | snp |
is | mentioned by |
dbSNP | rs6813479 |
dbSNP (classic) | rs6813479 |
ClinGen | rs6813479 |
ebi | rs6813479 |
HLI | rs6813479 |
Exac | rs6813479 |
Gnomad | rs6813479 |
Varsome | rs6813479 |
LitVar | rs6813479 |
Map | rs6813479 |
PheGenI | rs6813479 |
Biobank | rs6813479 |
1000 genomes | rs6813479 |
hgdp | rs6813479 |
ensembl | rs6813479 |
geneview | rs6813479 |
scholar | rs6813479 |
rs6813479 | |
pharmgkb | rs6813479 |
gwascentral | rs6813479 |
openSNP | rs6813479 |
23andMe | rs6813479 |
SNPshot | rs6813479 |
SNPdbe | rs6813479 |
MSV3d | rs6813479 |
GWAS Ctlg | rs6813479 |
GMAF | 0.4596 |
Max Magnitude | 0 |
? | (A;A) (A;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 |