rs1676232
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs1676232(A;A) |
| Make rs1676232(A;G) |
| Make rs1676232(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 117515992 |
| Gene | LOC105374056 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1676232 |
| dbSNP (classic) | rs1676232 |
| ClinGen | rs1676232 |
| ebi | rs1676232 |
| HLI | rs1676232 |
| Exac | rs1676232 |
| Gnomad | rs1676232 |
| Varsome | rs1676232 |
| LitVar | rs1676232 |
| Map | rs1676232 |
| PheGenI | rs1676232 |
| Biobank | rs1676232 |
| 1000 genomes | rs1676232 |
| hgdp | rs1676232 |
| ensembl | rs1676232 |
| geneview | rs1676232 |
| scholar | rs1676232 |
| rs1676232 | |
| pharmgkb | rs1676232 |
| gwascentral | rs1676232 |
| openSNP | rs1676232 |
| 23andMe | rs1676232 |
| SNPshot | rs1676232 |
| SNPdbe | rs1676232 |
| MSV3d | rs1676232 |
| GWAS Ctlg | rs1676232 |
| GMAF | 0.4013 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18318786
],AEHA 2008 ppt - rs4404477(A)/rs1676232(A) defines a significant left main coronary artery disease risk haplotype
