rs17431357
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common genotype |
Make rs17431357(C;T) |
Make rs17431357(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 120442631 |
Gene | TRIAP1 |
is a | snp |
is | mentioned by |
dbSNP | rs17431357 |
dbSNP (classic) | rs17431357 |
ClinGen | rs17431357 |
ebi | rs17431357 |
HLI | rs17431357 |
Exac | rs17431357 |
Gnomad | rs17431357 |
Varsome | rs17431357 |
LitVar | rs17431357 |
Map | rs17431357 |
PheGenI | rs17431357 |
Biobank | rs17431357 |
1000 genomes | rs17431357 |
hgdp | rs17431357 |
ensembl | rs17431357 |
geneview | rs17431357 |
scholar | rs17431357 |
rs17431357 | |
pharmgkb | rs17431357 |
gwascentral | rs17431357 |
openSNP | rs17431357 |
23andMe | rs17431357 |
SNPshot | rs17431357 |
SNPdbe | rs17431357 |
MSV3d | rs17431357 |
GWAS Ctlg | rs17431357 |
GMAF | 0.02984 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21901158] |
Trait | |
Title | Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. |
Risk Allele | C |
P-val | 0.000001 |
Odds Ratio | 34.0000 [22.00 - 44.00] % decrease |