Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs774047625
rs774047625
ERCC8 ; ERCC8-AS1
T 0.700 GeneticVariation CLINVAR RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease. 25525159

2015
dbSNP: rs774047625
rs774047625
ERCC8 ; ERCC8-AS1
T 0.700 GeneticVariation CLINVAR Cockayne syndrome type A: novel mutations in eight typical patients. 16865293

2006