rs779703983
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs779703983(G;G) |
| Make rs779703983(G;T) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 17 |
| Position | 80217046 |
| Gene | SGSH |
| is a | snp |
| is | mentioned by |
| dbSNP | rs779703983 |
| dbSNP (classic) | rs779703983 |
| ClinGen | rs779703983 |
| ebi | rs779703983 |
| HLI | rs779703983 |
| Exac | rs779703983 |
| Gnomad | rs779703983 |
| Varsome | rs779703983 |
| LitVar | rs779703983 |
| Map | rs779703983 |
| PheGenI | rs779703983 |
| Biobank | rs779703983 |
| 1000 genomes | rs779703983 |
| hgdp | rs779703983 |
| ensembl | rs779703983 |
| geneview | rs779703983 |
| scholar | rs779703983 |
| rs779703983 | |
| pharmgkb | rs779703983 |
| gwascentral | rs779703983 |
| openSNP | rs779703983 |
| 23andMe | rs779703983 |
| SNPshot | rs779703983 |
| SNPdbe | rs779703983 |
| MSV3d | rs779703983 |
| GWAS Ctlg | rs779703983 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs779703983(G;G) |
| Alt | rs779703983(G;G) |
| Reference | Rs779703983(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | SGSH |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000017.10:g.78190845T>G |
| CLNSRC | |
| CLNACC | RCV000413476.1, |
