rs1642742
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs1642742(C;T) |
| Make rs1642742(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 3 |
| Position | 10150259 |
| Gene | VHL |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1642742 |
| dbSNP (classic) | rs1642742 |
| ClinGen | rs1642742 |
| ebi | rs1642742 |
| HLI | rs1642742 |
| Exac | rs1642742 |
| Gnomad | rs1642742 |
| Varsome | rs1642742 |
| LitVar | rs1642742 |
| Map | rs1642742 |
| PheGenI | rs1642742 |
| Biobank | rs1642742 |
| 1000 genomes | rs1642742 |
| hgdp | rs1642742 |
| ensembl | rs1642742 |
| geneview | rs1642742 |
| scholar | rs1642742 |
| rs1642742 | |
| pharmgkb | rs1642742 |
| gwascentral | rs1642742 |
| openSNP | rs1642742 |
| 23andMe | rs1642742 |
| SNPshot | rs1642742 |
| SNPdbe | rs1642742 |
| MSV3d | rs1642742 |
| GWAS Ctlg | rs1642742 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 25217002
] Two single nucleotide polymorphisms in the von Hippel-Lindau tumor suppressor gene in Taiwanese with renal cell carcinoma
| ClinVar | |
|---|---|
| Risk | rs1642742(T;T) |
| Alt | rs1642742(T;T) |
| Reference | Rs1642742(C;C) |
| Significance | Non-pathogenic |
| Disease | Von Hippel-Lindau syndrome |
| Variation | info |
| Gene | VHL |
| CLNDBN | Von Hippel-Lindau syndrome |
| Reversed | 1 |
| HGVS | NC_000003.11:g.10191943G>A |
| CLNSRC | |
| CLNACC | RCV000348075.1, |
