rs61745150
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61745150(A;A) |
| Make rs61745150(A;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 15 |
| Position | 27990589 |
| Gene | OCA2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61745150 |
| dbSNP (classic) | rs61745150 |
| ClinGen | rs61745150 |
| ebi | rs61745150 |
| HLI | rs61745150 |
| Exac | rs61745150 |
| Gnomad | rs61745150 |
| Varsome | rs61745150 |
| LitVar | rs61745150 |
| Map | rs61745150 |
| PheGenI | rs61745150 |
| Biobank | rs61745150 |
| 1000 genomes | rs61745150 |
| hgdp | rs61745150 |
| ensembl | rs61745150 |
| geneview | rs61745150 |
| scholar | rs61745150 |
| rs61745150 | |
| pharmgkb | rs61745150 |
| gwascentral | rs61745150 |
| openSNP | rs61745150 |
| 23andMe | rs61745150 |
| SNPshot | rs61745150 |
| SNPdbe | rs61745150 |
| MSV3d | rs61745150 |
| GWAS Ctlg | rs61745150 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61745150(A;A) |
| Alt | rs61745150(A;A) |
| Reference | Rs61745150(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not specified not provided |
| Variation | info |
| Gene | OCA2 |
| CLNDBN | not specified not provided |
| Reversed | 0 |
| HGVS | NC_000015.9:g.28235735G>A |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000173667.1, RCV000442309.1, |
