rs935526225
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs935526225(A;A) |
| Make rs935526225(A;G) |
| Make rs935526225(G;G) |
| Reference | GRCh38.p7 38.3/150 |
| Chromosome | 11 |
| Position | 6616521 |
| Gene | TPP1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs935526225 |
| dbSNP (classic) | rs935526225 |
| ClinGen | rs935526225 |
| ebi | rs935526225 |
| HLI | rs935526225 |
| Exac | rs935526225 |
| Gnomad | rs935526225 |
| Varsome | rs935526225 |
| LitVar | rs935526225 |
| Map | rs935526225 |
| PheGenI | rs935526225 |
| Biobank | rs935526225 |
| 1000 genomes | rs935526225 |
| hgdp | rs935526225 |
| ensembl | rs935526225 |
| geneview | rs935526225 |
| scholar | rs935526225 |
| rs935526225 | |
| pharmgkb | rs935526225 |
| gwascentral | rs935526225 |
| openSNP | rs935526225 |
| 23andMe | rs935526225 |
| SNPshot | rs935526225 |
| SNPdbe | rs935526225 |
| MSV3d | rs935526225 |
| GWAS Ctlg | rs935526225 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs935526225(C;C) |
| Alt | rs935526225(C;C) |
| Reference | Rs935526225(T;T) |
| Significance | Probable-Pathogenic |
| Disease | not provided |
| Variation | info |
| Gene | TPP1 |
| CLNDBN | not provided |
| Reversed | 0 |
| HGVS | NC_000011.9:g.6637752T>C |
| CLNSRC | |
| CLNACC | RCV000428562.1, |
