rs79843600
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs79843600(C;T) |
| Make rs79843600(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 19 |
| Position | 12813164 |
| Gene | RNASEH2A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs79843600 |
| dbSNP (classic) | rs79843600 |
| ClinGen | rs79843600 |
| ebi | rs79843600 |
| HLI | rs79843600 |
| Exac | rs79843600 |
| Gnomad | rs79843600 |
| Varsome | rs79843600 |
| LitVar | rs79843600 |
| Map | rs79843600 |
| PheGenI | rs79843600 |
| Biobank | rs79843600 |
| 1000 genomes | rs79843600 |
| hgdp | rs79843600 |
| ensembl | rs79843600 |
| geneview | rs79843600 |
| scholar | rs79843600 |
| rs79843600 | |
| pharmgkb | rs79843600 |
| gwascentral | rs79843600 |
| openSNP | rs79843600 |
| 23andMe | rs79843600 |
| SNPshot | rs79843600 |
| SNPdbe | rs79843600 |
| MSV3d | rs79843600 |
| GWAS Ctlg | rs79843600 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs79843600(G;G) rs79843600(T;T) |
| Alt | rs79843600(G;G) rs79843600(T;T) |
| Reference | Rs79843600(C;C) |
| Significance | Pathogenic |
| Disease | Aicardi Goutieres syndrome 4 |
| Variation | info |
| Gene | RNASEH2A |
| CLNDBN | Aicardi Goutieres syndrome 4 |
| Reversed | 0 |
| HGVS | NC_000019.9:g.12923978C>T |
| CLNSRC | UniProtKB (protein) |
| CLNACC | RCV000114341.2, |
