Disease: Xeroderma pigmentosum, group F ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1799798
rs1799798
Entrez Id: 2072
Gene Symbol: ERCC4
ERCC4
CUI: C0268140
Disease:
Xeroderma pigmentosum, group F 		0.010 GeneticVariation BEFREE However, we did not find an association with increased risk of glioma for the polymorphisms rs3136038, rs1799798, and rs2276466 in XPF. 24938470 2014