rs763162812
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs763162812(A;A) |
| Make rs763162812(A;T) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 6616720 |
| Gene | TPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs763162812 |
| dbSNP (classic) | rs763162812 |
| ClinGen | rs763162812 |
| ebi | rs763162812 |
| HLI | rs763162812 |
| Exac | rs763162812 |
| Gnomad | rs763162812 |
| Varsome | rs763162812 |
| LitVar | rs763162812 |
| Map | rs763162812 |
| PheGenI | rs763162812 |
| Biobank | rs763162812 |
| 1000 genomes | rs763162812 |
| hgdp | rs763162812 |
| ensembl | rs763162812 |
| geneview | rs763162812 |
| scholar | rs763162812 |
| rs763162812 | |
| pharmgkb | rs763162812 |
| gwascentral | rs763162812 |
| openSNP | rs763162812 |
| 23andMe | rs763162812 |
| SNPshot | rs763162812 |
| SNPdbe | rs763162812 |
| MSV3d | rs763162812 |
| GWAS Ctlg | rs763162812 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs763162812(A;A) |
| Alt | rs763162812(A;A) |
| Reference | Rs763162812(T;T) |
| Significance | Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TPP1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.6637951T>A |
| CLNSRC | |
| CLNACC | RCV000189773.1, |
