rs1870134
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs1870134(C;C) |
Make rs1870134(C;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 14178523 |
Gene | LSM3, XPC |
is a | snp |
is | mentioned by |
dbSNP | rs1870134 |
dbSNP (classic) | rs1870134 |
ClinGen | rs1870134 |
ebi | rs1870134 |
HLI | rs1870134 |
Exac | rs1870134 |
Gnomad | rs1870134 |
Varsome | rs1870134 |
LitVar | rs1870134 |
Map | rs1870134 |
PheGenI | rs1870134 |
Biobank | rs1870134 |
1000 genomes | rs1870134 |
hgdp | rs1870134 |
ensembl | rs1870134 |
geneview | rs1870134 |
scholar | rs1870134 |
rs1870134 | |
pharmgkb | rs1870134 |
gwascentral | rs1870134 |
openSNP | rs1870134 |
23andMe | rs1870134 |
SNPshot | rs1870134 |
SNPdbe | rs1870134 |
MSV3d | rs1870134 |
GWAS Ctlg | rs1870134 |
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 | rs1870134(C;C) rs1870134(T;T) |
Alt | rs1870134(C;C) rs1870134(T;T) |
Reference | Rs1870134(G;G) |
Significance | Non-pathogenic |
Disease | not specified Xeroderma pigmentosum |
Variation | info |
Gene | LSM3 XPC |
CLNDBN | not specified Xeroderma pigmentosum |
Reversed | 0 |
HGVS | NC_000003.11:g.14220023G>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000122323.3, RCV000333184.1, |
[PMID 31333776] Associations of mRNA expression of DNA repair genes and genetic polymorphisms with cancer risk: a bioinformatics analysis and meta-analysis.