rs750428882
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs750428882(A;A) |
| Make rs750428882(A;G) |
| Reference | GRCh38.p2 38.2/146 |
| Chromosome | 11 |
| Position | 6616375 |
| Gene | TPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs750428882 |
| dbSNP (classic) | rs750428882 |
| ClinGen | rs750428882 |
| ebi | rs750428882 |
| HLI | rs750428882 |
| Exac | rs750428882 |
| Gnomad | rs750428882 |
| Varsome | rs750428882 |
| LitVar | rs750428882 |
| Map | rs750428882 |
| PheGenI | rs750428882 |
| Biobank | rs750428882 |
| 1000 genomes | rs750428882 |
| hgdp | rs750428882 |
| ensembl | rs750428882 |
| geneview | rs750428882 |
| scholar | rs750428882 |
| rs750428882 | |
| pharmgkb | rs750428882 |
| gwascentral | rs750428882 |
| openSNP | rs750428882 |
| 23andMe | rs750428882 |
| SNPshot | rs750428882 |
| SNPdbe | rs750428882 |
| MSV3d | rs750428882 |
| GWAS Ctlg | rs750428882 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs750428882(A;A) rs750428882(C;C) |
| Alt | rs750428882(A;A) rs750428882(C;C) |
| Reference | Rs750428882(G;G) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TPP1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.6637606G>A |
| CLNSRC | |
| CLNACC | RCV000189779.2, |
