Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs745659712
rs745659712
Entrez Id: 5965
Gene Symbol: RECQL
RECQL
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary
CT 0.700 CausalMutation CLINVAR