rs254942
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(T;T) | 0 | common genotype |
Make rs254942(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 13932150 |
Gene | ERCC4 |
is a | snp |
is | mentioned by |
dbSNP | rs254942 |
dbSNP (classic) | rs254942 |
ClinGen | rs254942 |
ebi | rs254942 |
HLI | rs254942 |
Exac | rs254942 |
Gnomad | rs254942 |
Varsome | rs254942 |
LitVar | rs254942 |
Map | rs254942 |
PheGenI | rs254942 |
Biobank | rs254942 |
1000 genomes | rs254942 |
hgdp | rs254942 |
ensembl | rs254942 |
geneview | rs254942 |
scholar | rs254942 |
rs254942 | |
pharmgkb | rs254942 |
gwascentral | rs254942 |
openSNP | rs254942 |
23andMe | rs254942 |
SNPshot | rs254942 |
SNPdbe | rs254942 |
MSV3d | rs254942 |
GWAS Ctlg | rs254942 |
GMAF | 0.06933 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23415627] Association of two ERCC4 tagSNPs with susceptibility to atrophic gastritis and gastric cancer in Chinese
ClinVar | |
---|---|
Risk | rs254942(A;A) Rs254942(T;T) |
Alt | rs254942(A;A) Rs254942(T;T) |
Reference | Rs254942(C;C) |
Significance | Non-pathogenic |
Disease | not specified Xeroderma pigmentosum |
Variation | info |
Gene | ERCC4 |
CLNDBN | not specified Xeroderma pigmentosum |
Reversed | 1 |
HGVS | NC_000016.9:g.14026007G>A |
CLNSRC | |
CLNACC | RCV000246561.1, RCV000318579.1, |