rs121965092
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs121965092(A;A) |
Make rs121965092(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 14145785 |
Gene | XPC |
is a | snp |
is | mentioned by |
dbSNP | rs121965092 |
dbSNP (classic) | rs121965092 |
ClinGen | rs121965092 |
ebi | rs121965092 |
HLI | rs121965092 |
Exac | rs121965092 |
Gnomad | rs121965092 |
Varsome | rs121965092 |
LitVar | rs121965092 |
Map | rs121965092 |
PheGenI | rs121965092 |
Biobank | rs121965092 |
1000 genomes | rs121965092 |
hgdp | rs121965092 |
ensembl | rs121965092 |
geneview | rs121965092 |
scholar | rs121965092 |
rs121965092 | |
pharmgkb | rs121965092 |
gwascentral | rs121965092 |
openSNP | rs121965092 |
23andMe | rs121965092 |
SNPshot | rs121965092 |
SNPdbe | rs121965092 |
MSV3d | rs121965092 |
GWAS Ctlg | rs121965092 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121965092(A;A) |
Alt | rs121965092(A;A) |
Reference | Rs121965092(G;G) |
Significance | Probable-Pathogenic |
Disease | Malignant tumor of urinary bladder |
Variation | info |
Gene | XPC |
CLNDBN | Malignant tumor of urinary bladder |
Reversed | 1 |
HGVS | NC_000003.11:g.14187285C>T |
CLNSRC | |
CLNACC |
[PMID 21273643] In vitro functional effects of XPC gene rare variants from bladder cancer patients.