rs896431562
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 0 | common in clinvar |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 8 |
| Position | 74350550 |
| Gene | GDAP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs896431562 |
| dbSNP (classic) | rs896431562 |
| ClinGen | rs896431562 |
| ebi | rs896431562 |
| HLI | rs896431562 |
| Exac | rs896431562 |
| Gnomad | rs896431562 |
| Varsome | rs896431562 |
| LitVar | rs896431562 |
| Map | rs896431562 |
| PheGenI | rs896431562 |
| Biobank | rs896431562 |
| 1000 genomes | rs896431562 |
| hgdp | rs896431562 |
| ensembl | rs896431562 |
| geneview | rs896431562 |
| scholar | rs896431562 |
| rs896431562 | |
| pharmgkb | rs896431562 |
| gwascentral | rs896431562 |
| openSNP | rs896431562 |
| 23andMe | rs896431562 |
| SNPshot | rs896431562 |
| SNPdbe | rs896431562 |
| MSV3d | rs896431562 |
| GWAS Ctlg | rs896431562 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs896431562(T;T) |
| Alt | rs896431562(T;T) |
| Reference | Rs896431562(A;A) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | GDAP1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000008.10:g.75262785A>T |
| CLNSRC | |
| CLNACC | RCV000482807.1, |
