rs761796175
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs761796175(A;A) |
| Make rs761796175(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 2 |
| Position | 237377336 |
| Gene | COL6A3 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs761796175 |
| dbSNP (classic) | rs761796175 |
| ClinGen | rs761796175 |
| ebi | rs761796175 |
| HLI | rs761796175 |
| Exac | rs761796175 |
| Gnomad | rs761796175 |
| Varsome | rs761796175 |
| LitVar | rs761796175 |
| Map | rs761796175 |
| PheGenI | rs761796175 |
| Biobank | rs761796175 |
| 1000 genomes | rs761796175 |
| hgdp | rs761796175 |
| ensembl | rs761796175 |
| geneview | rs761796175 |
| scholar | rs761796175 |
| rs761796175 | |
| pharmgkb | rs761796175 |
| gwascentral | rs761796175 |
| openSNP | rs761796175 |
| 23andMe | rs761796175 |
| SNPshot | rs761796175 |
| SNPdbe | rs761796175 |
| MSV3d | rs761796175 |
| GWAS Ctlg | rs761796175 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs761796175(A;A) |
| Alt | rs761796175(A;A) |
| Reference | Rs761796175(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | COL6A3 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.238285979G>A |
| CLNSRC | |
| CLNACC | RCV000482545.1, |
