rs121965090
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs121965090(C;T) |
| Make rs121965090(T;T) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 3 |
| Position | 14158706 |
| Gene | XPC |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121965090 |
| dbSNP (classic) | rs121965090 |
| ClinGen | rs121965090 |
| ebi | rs121965090 |
| HLI | rs121965090 |
| Exac | rs121965090 |
| Gnomad | rs121965090 |
| Varsome | rs121965090 |
| LitVar | rs121965090 |
| Map | rs121965090 |
| PheGenI | rs121965090 |
| Biobank | rs121965090 |
| 1000 genomes | rs121965090 |
| hgdp | rs121965090 |
| ensembl | rs121965090 |
| geneview | rs121965090 |
| scholar | rs121965090 |
| rs121965090 | |
| pharmgkb | rs121965090 |
| gwascentral | rs121965090 |
| openSNP | rs121965090 |
| 23andMe | rs121965090 |
| SNPshot | rs121965090 |
| SNPdbe | rs121965090 |
| MSV3d | rs121965090 |
| GWAS Ctlg | rs121965090 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121965090(T;T) |
| Alt | rs121965090(T;T) |
| Reference | Rs121965090(C;C) |
| Significance | Untested |
| Disease | not specified |
| Variation | info |
| Gene | XPC |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000003.11:g.14200206G>A |
| CLNSRC | ClinVar |
| CLNACC | RCV000122342.1, |
[PMID 21273643
] In vitro functional effects of XPC gene rare variants from bladder cancer patients.
