Variant: rs121434325 

    present in Gene: ERCC8
    present in Chromosome: 5
    Position on Chromosome: 60904794
    Alleles of this Variant: G/A

rs121434325 in ERCC8 gene and Cockayne Syndrome, Type I PMID 14661080 2004 CKN1 (MIM 216400): mutations in Cockayne syndrome type A and a new common polymorphism.

PMID 19894250 2010 Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.

PMID 15744458 2005 Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects.