rs146795445
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;T) | 3 | carrier of a cystic fibrosis allele |
| (T;T) | 0 | common in clinvar |
| Make rs146795445(C;C) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 117642595 |
| Gene | CFTR |
| is a | snp |
| is | mentioned by |
| dbSNP | rs146795445 |
| dbSNP (classic) | rs146795445 |
| ClinGen | rs146795445 |
| ebi | rs146795445 |
| HLI | rs146795445 |
| Exac | rs146795445 |
| Gnomad | rs146795445 |
| Varsome | rs146795445 |
| LitVar | rs146795445 |
| Map | rs146795445 |
| PheGenI | rs146795445 |
| Biobank | rs146795445 |
| 1000 genomes | rs146795445 |
| hgdp | rs146795445 |
| ensembl | rs146795445 |
| geneview | rs146795445 |
| scholar | rs146795445 |
| rs146795445 | |
| pharmgkb | rs146795445 |
| gwascentral | rs146795445 |
| openSNP | rs146795445 |
| 23andMe | rs146795445 |
| SNPshot | rs146795445 |
| SNPdbe | rs146795445 |
| MSV3d | rs146795445 |
| GWAS Ctlg | rs146795445 |
| Max Magnitude | 3 |
| ClinVar | |
|---|---|
| Risk | rs146795445(C;C) |
| Alt | rs146795445(C;C) |
| Reference | Rs146795445(T;T) |
| Significance | Untested |
| Disease | Cystic fibrosis |
| Variation | info |
| Gene | CFTR |
| CLNDBN | Cystic fibrosis |
| Reversed | 0 |
| HGVS | NC_000007.13:g.117282649T>C |
| CLNSRC | ClinVar |
| CLNACC | RCV000047004.2, |
