rs61749438
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs61749438(A;A) |
| Make rs61749438(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 94055133 |
| Gene | ABCA4 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs61749438 |
| dbSNP (classic) | rs61749438 |
| ClinGen | rs61749438 |
| ebi | rs61749438 |
| HLI | rs61749438 |
| Exac | rs61749438 |
| Gnomad | rs61749438 |
| Varsome | rs61749438 |
| LitVar | rs61749438 |
| Map | rs61749438 |
| PheGenI | rs61749438 |
| Biobank | rs61749438 |
| 1000 genomes | rs61749438 |
| hgdp | rs61749438 |
| ensembl | rs61749438 |
| geneview | rs61749438 |
| scholar | rs61749438 |
| rs61749438 | |
| pharmgkb | rs61749438 |
| gwascentral | rs61749438 |
| openSNP | rs61749438 |
| 23andMe | rs61749438 |
| SNPshot | rs61749438 |
| SNPdbe | rs61749438 |
| MSV3d | rs61749438 |
| GWAS Ctlg | rs61749438 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs61749438(A;A) |
| Alt | rs61749438(A;A) |
| Reference | Rs61749438(G;G) |
| Significance | Pathogenic |
| Disease | Stargardt disease 1 not provided |
| Variation | info |
| Gene | ABCA4 |
| CLNDBN | Stargardt disease 1 not provided |
| Reversed | 1 |
| HGVS | NC_000001.10:g.94520689C>T |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000008334.5, RCV000085489.1, |
