rs59985777
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs59985777(C;C) |
| Make rs59985777(C;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 17 |
| Position | 44911371 |
| Gene | GFAP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs59985777 |
| dbSNP (classic) | rs59985777 |
| ClinGen | rs59985777 |
| ebi | rs59985777 |
| HLI | rs59985777 |
| Exac | rs59985777 |
| Gnomad | rs59985777 |
| Varsome | rs59985777 |
| LitVar | rs59985777 |
| Map | rs59985777 |
| PheGenI | rs59985777 |
| Biobank | rs59985777 |
| 1000 genomes | rs59985777 |
| hgdp | rs59985777 |
| ensembl | rs59985777 |
| geneview | rs59985777 |
| scholar | rs59985777 |
| rs59985777 | |
| pharmgkb | rs59985777 |
| gwascentral | rs59985777 |
| openSNP | rs59985777 |
| 23andMe | rs59985777 |
| SNPshot | rs59985777 |
| SNPdbe | rs59985777 |
| MSV3d | rs59985777 |
| GWAS Ctlg | rs59985777 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs59985777(C;C) |
| Alt | rs59985777(C;C) |
| Reference | Rs59985777(T;T) |
| Significance | Pathogenic |
| Disease | not provided Alexander's disease |
| Variation | info |
| Gene | GFAP |
| CLNDBN | not provided Alexander's disease |
| Reversed | 1 |
| HGVS | NC_000017.10:g.42988739A>G |
| CLNSRC | |
| CLNACC | RCV000056918.1, RCV000192153.1, |
