rs238417
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs238417(C;G) |
Make rs238417(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 19 |
Position | 45353210 |
Gene | ERCC2 |
is a | snp |
is | mentioned by |
dbSNP | rs238417 |
dbSNP (classic) | rs238417 |
ClinGen | rs238417 |
ebi | rs238417 |
HLI | rs238417 |
Exac | rs238417 |
Gnomad | rs238417 |
Varsome | rs238417 |
LitVar | rs238417 |
Map | rs238417 |
PheGenI | rs238417 |
Biobank | rs238417 |
1000 genomes | rs238417 |
hgdp | rs238417 |
ensembl | rs238417 |
geneview | rs238417 |
scholar | rs238417 |
rs238417 | |
pharmgkb | rs238417 |
gwascentral | rs238417 |
openSNP | rs238417 |
23andMe | rs238417 |
SNPshot | rs238417 |
SNPdbe | rs238417 |
MSV3d | rs238417 |
GWAS Ctlg | rs238417 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
[PMID 26967386] The association of six polymorphisms of five genes involved in three steps of nucleotide excision repair pathways with hepatocellular cancer risk.
ClinVar | |
---|---|
Risk | rs238417(A;A) rs238417(G;G) |
Alt | rs238417(A;A) rs238417(G;G) |
Reference | Rs238417(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | ERCC2 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000019.9:g.45856468G>C |
CLNSRC | |
CLNACC | RCV000253904.1, |