rs76642637
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs76642637(-;-) |
| Make rs76642637(-;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 48467155 |
| Gene | TREX1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs76642637 |
| dbSNP (classic) | rs76642637 |
| ClinGen | rs76642637 |
| ebi | rs76642637 |
| HLI | rs76642637 |
| Exac | rs76642637 |
| Gnomad | rs76642637 |
| Varsome | rs76642637 |
| LitVar | rs76642637 |
| Map | rs76642637 |
| PheGenI | rs76642637 |
| Biobank | rs76642637 |
| 1000 genomes | rs76642637 |
| hgdp | rs76642637 |
| ensembl | rs76642637 |
| geneview | rs76642637 |
| scholar | rs76642637 |
| rs76642637 | |
| pharmgkb | rs76642637 |
| gwascentral | rs76642637 |
| openSNP | rs76642637 |
| 23andMe | rs76642637 |
| SNPshot | rs76642637 |
| SNPdbe | rs76642637 |
| MSV3d | rs76642637 |
| GWAS Ctlg | rs76642637 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs76642637(-;-) |
| Alt | rs76642637(-;-) |
| Reference | Rs76642637(G;G) |
| Significance | Pathogenic |
| Disease | Aicardi Goutieres syndrome 1 |
| Variation | info |
| Gene | ATRIP TREX1 |
| CLNDBN | Aicardi Goutieres syndrome 1 |
| Reversed | 0 |
| HGVS | NC_000003.11:g.48508554delG |
| CLNSRC | ClinVar |
| CLNACC | RCV000114328.3, |
