rs112005636
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Make rs112005636(A;G) |
| Make rs112005636(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 1 |
| Position | 93996107 |
| Gene | ABCA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs112005636 |
| dbSNP (classic) | rs112005636 |
| ClinGen | rs112005636 |
| ebi | rs112005636 |
| HLI | rs112005636 |
| Exac | rs112005636 |
| Gnomad | rs112005636 |
| Varsome | rs112005636 |
| LitVar | rs112005636 |
| Map | rs112005636 |
| PheGenI | rs112005636 |
| Biobank | rs112005636 |
| 1000 genomes | rs112005636 |
| hgdp | rs112005636 |
| ensembl | rs112005636 |
| geneview | rs112005636 |
| scholar | rs112005636 |
| rs112005636 | |
| pharmgkb | rs112005636 |
| gwascentral | rs112005636 |
| openSNP | rs112005636 |
| 23andMe | rs112005636 |
| SNPshot | rs112005636 |
| SNPdbe | rs112005636 |
| MSV3d | rs112005636 |
| GWAS Ctlg | rs112005636 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs112005636(G;G) rs112005636(T;T) |
| Alt | rs112005636(G;G) rs112005636(T;T) |
| Reference | Rs112005636(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | ABCA4 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000001.10:g.94461663A>T |
| CLNSRC | |
| CLNACC | RCV000487635.1, |
