rs532007026
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs532007026(C;G) |
| Make rs532007026(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 3 |
| Position | 25733983 |
| Gene | NGLY1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs532007026 |
| dbSNP (classic) | rs532007026 |
| ClinGen | rs532007026 |
| ebi | rs532007026 |
| HLI | rs532007026 |
| Exac | rs532007026 |
| Gnomad | rs532007026 |
| Varsome | rs532007026 |
| LitVar | rs532007026 |
| Map | rs532007026 |
| PheGenI | rs532007026 |
| Biobank | rs532007026 |
| 1000 genomes | rs532007026 |
| hgdp | rs532007026 |
| ensembl | rs532007026 |
| geneview | rs532007026 |
| scholar | rs532007026 |
| rs532007026 | |
| pharmgkb | rs532007026 |
| gwascentral | rs532007026 |
| openSNP | rs532007026 |
| 23andMe | rs532007026 |
| SNPshot | rs532007026 |
| SNPdbe | rs532007026 |
| MSV3d | rs532007026 |
| GWAS Ctlg | rs532007026 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs532007026(G;G) |
| Alt | rs532007026(G;G) |
| Reference | Rs532007026(C;C) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | NGLY1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000003.11:g.25775474C>G |
| CLNSRC | |
| CLNACC | RCV000413780.1, |
