rs1401492
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs1401492(A;A) |
Make rs1401492(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 53646097 |
Gene | CACNA1D |
is a | snp |
is | mentioned by |
dbSNP | rs1401492 |
dbSNP (classic) | rs1401492 |
ClinGen | rs1401492 |
ebi | rs1401492 |
HLI | rs1401492 |
Exac | rs1401492 |
Gnomad | rs1401492 |
Varsome | rs1401492 |
LitVar | rs1401492 |
Map | rs1401492 |
PheGenI | rs1401492 |
Biobank | rs1401492 |
1000 genomes | rs1401492 |
hgdp | rs1401492 |
ensembl | rs1401492 |
geneview | rs1401492 |
scholar | rs1401492 |
rs1401492 | |
pharmgkb | rs1401492 |
gwascentral | rs1401492 |
openSNP | rs1401492 |
23andMe | rs1401492 |
SNPshot | rs1401492 |
SNPdbe | rs1401492 |
MSV3d | rs1401492 |
GWAS Ctlg | rs1401492 |
GMAF | 0.05372 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | 0.000005 |
Odds Ratio | 16.0000 [9.00 - 22.00] % decrease |