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rs873601

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs873601(A;A)
Make rs873601(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position102875987
GeneBIVM-ERCC5, ERCC5
is asnp
is mentioned by
dbSNPrs873601
dbSNP (classic)rs873601
ClinGenrs873601
ebirs873601
HLIrs873601
Exacrs873601
Gnomadrs873601
Varsomers873601
LitVarrs873601
Maprs873601
PheGenIrs873601
Biobankrs873601
1000 genomesrs873601
hgdprs873601
ensemblrs873601
geneviewrs873601
scholarrs873601
googlers873601
pharmgkbrs873601
gwascentralrs873601
openSNPrs873601
23andMers873601
SNPshotrs873601
SNPdbers873601
MSV3drs873601
GWAS Ctlgrs873601
GMAF0.4559
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 24353624OA-icon.png] XPG is a novel biomarker of clinical outcome in advanced non-small-cell lung cancer


[PMID 22371296] Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.


[PMID 26967386OA-icon.png] The association of six polymorphisms of five genes involved in three steps of nucleotide excision repair pathways with hepatocellular cancer risk.


[PMID 27228234] XPG Gene Polymorphisms and the Risk of Gastric Cardiac Adenocarcinoma.


[PMID 27235448OA-icon.png] Haplotype and diplotype analyses of variation in ERCC5 transcription cis-regulation in normal bronchial epithelial cells.


ClinVar
Risk rs873601(A;A)
Alt rs873601(A;A)
Reference Rs873601(G;G)
Significance Non-pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene BIVM-ERCC5 ERCC5
CLNDBN Xeroderma pigmentosum
Reversed 0
HGVS NC_000013.10:g.103528337G>A
CLNSRC
CLNACC RCV000342790.1,



[PMID 28952217] Study on association between ERCC5 single nucleotide polymorphism and susceptibility to esophageal cancer.


[PMID 29434449OA-icon.png] Impact of SNP-SNP interactions of DNA repair gene ERCC5 and metabolic gene GSTP1 on gastric cancer/atrophic gastritis risk in a Chinese population.


[PMID 29506519OA-icon.png] RNAseq analysis of bronchial epithelial cells to identify COPD-associated genes and SNPs.


[PMID 30139812OA-icon.png] XPG polymorphisms rs873601 G>A contributes to uterine leiomyoma susceptibility in a Southern Chinese population.


[PMID 33393424] XPG gene polymorphisms and glioma susceptibility: a two-center case-control study.