Disease: Cockayne Syndrome, Type I ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554076239
rs1554076239
Entrez Id: 1161;91942
Gene Symbol: ERCC8;NDUFAF2
ERCC8;NDUFAF2
CUI: C0751039
Disease:
Cockayne Syndrome, Type I 		C 0.700 GeneticVariation CLINVAR