rs75186889
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs75186889(-;-) |
| Make rs75186889(-;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 13 |
| Position | 50927479 |
| Gene | RNASEH2B |
| is a | snp |
| is | mentioned by |
| dbSNP | rs75186889 |
| dbSNP (classic) | rs75186889 |
| ClinGen | rs75186889 |
| ebi | rs75186889 |
| HLI | rs75186889 |
| Exac | rs75186889 |
| Gnomad | rs75186889 |
| Varsome | rs75186889 |
| LitVar | rs75186889 |
| Map | rs75186889 |
| PheGenI | rs75186889 |
| Biobank | rs75186889 |
| 1000 genomes | rs75186889 |
| hgdp | rs75186889 |
| ensembl | rs75186889 |
| geneview | rs75186889 |
| scholar | rs75186889 |
| rs75186889 | |
| pharmgkb | rs75186889 |
| gwascentral | rs75186889 |
| openSNP | rs75186889 |
| 23andMe | rs75186889 |
| SNPshot | rs75186889 |
| SNPdbe | rs75186889 |
| MSV3d | rs75186889 |
| GWAS Ctlg | rs75186889 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | |
| Alt | |
| Reference | Rs75186889(G;G) |
| Significance | Pathogenic |
| Disease | Aicardi Goutieres syndrome 2 |
| Variation | info |
| Gene | RNASEH2B |
| CLNDBN | Aicardi Goutieres syndrome 2 |
| Reversed | 0 |
| HGVS | NC_000013.10:g.51501615delG |
| CLNSRC | |
| CLNACC | |
