rs767707248
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs767707248(A;A) |
| Make rs767707248(A;G) |
| Reference | GRCh38.p7 38.3/149 |
| Chromosome | 2 |
| Position | 215064205 |
| Gene | ABCA12 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs767707248 |
| dbSNP (classic) | rs767707248 |
| ClinGen | rs767707248 |
| ebi | rs767707248 |
| HLI | rs767707248 |
| Exac | rs767707248 |
| Gnomad | rs767707248 |
| Varsome | rs767707248 |
| LitVar | rs767707248 |
| Map | rs767707248 |
| PheGenI | rs767707248 |
| Biobank | rs767707248 |
| 1000 genomes | rs767707248 |
| hgdp | rs767707248 |
| ensembl | rs767707248 |
| geneview | rs767707248 |
| scholar | rs767707248 |
| rs767707248 | |
| pharmgkb | rs767707248 |
| gwascentral | rs767707248 |
| openSNP | rs767707248 |
| 23andMe | rs767707248 |
| SNPshot | rs767707248 |
| SNPdbe | rs767707248 |
| MSV3d | rs767707248 |
| GWAS Ctlg | rs767707248 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs767707248(A;A) |
| Alt | rs767707248(A;A) |
| Reference | Rs767707248(G;G) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ABCA12 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000002.11:g.215928928G>A |
| CLNSRC | |
| CLNACC | RCV000255481.1, |
