Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569083679
rs1569083679
Entrez Id: 2187
Gene Symbol: FANCB
FANCB
CUI: C1845292
Disease:
FANCONI ANEMIA, COMPLEMENTATION GROUP B
C 0.700 CausalMutation CLINVAR Genetic subtyping of Fanconi anemia by comprehensive mutation screening. 17924555 2008
dbSNP: rs1569083679
rs1569083679
Entrez Id: 2187
Gene Symbol: FANCB
FANCB
CUI: C1845292
Disease:
FANCONI ANEMIA, COMPLEMENTATION GROUP B
C 0.700 CausalMutation CLINVAR X-linked inheritance of Fanconi anemia complementation group B. 15502827 2004