rs1800067 is a SNP in the ERCC4 gene. it is significantly associated with cancer risk.

Significantly increased meningioma risk was observed for the minor allele ''A'' (P= 0.01) [R]. 

Individuals carrying the GG genotype were more likely to have an increased risk of glioma when compared with carriers of the A/A genotype in a co-dominant model (OR= 2.85) [R].

''A'' allele and the A/G genotype were significantly associated with a decreased risk of lung cancer compared to the G allele (OR=0.806, P=0.003) [R]. 

''A'' allele was significantly associated with a decreased risk of glioma [R].

 

rs1800067

Parent Gene: ERCC4

Importance: 2
Less common allele: A = 3%
More common allele: G = 97%
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