rs62637016
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (AG;AG) | 0 | common in clinvar |
| (I;I) | 0 |
| Make rs62637016(-;-) |
| Make rs62637016(-;AG) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 17 |
| Position | 6425604 |
| Gene | AIPL1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs62637016 |
| dbSNP (classic) | rs62637016 |
| ClinGen | rs62637016 |
| ebi | rs62637016 |
| HLI | rs62637016 |
| Exac | rs62637016 |
| Gnomad | rs62637016 |
| Varsome | rs62637016 |
| LitVar | rs62637016 |
| Map | rs62637016 |
| PheGenI | rs62637016 |
| Biobank | rs62637016 |
| 1000 genomes | rs62637016 |
| hgdp | rs62637016 |
| ensembl | rs62637016 |
| geneview | rs62637016 |
| scholar | rs62637016 |
| rs62637016 | |
| pharmgkb | rs62637016 |
| gwascentral | rs62637016 |
| openSNP | rs62637016 |
| 23andMe | rs62637016 |
| SNPshot | rs62637016 |
| SNPdbe | rs62637016 |
| MSV3d | rs62637016 |
| GWAS Ctlg | rs62637016 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs62637016(-;-) |
| Alt | rs62637016(-;-) |
| Reference | Rs62637016(AG;AG) |
| Significance | Pathogenic |
| Disease | Leber congenital amaurosis 4 not provided |
| Variation | info |
| Gene | AIPL1 |
| CLNDBN | Leber congenital amaurosis 4 not provided |
| Reversed | 1 |
| HGVS | NC_000017.10:g.6328924_6328925delCT |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000005907.2, RCV000086209.1, |
