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 |
