rs1291524243, FANCA

N. diseases: 2
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
CUI: C3469521
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder)
0.700 GeneticVariation CLINVAR Reverse mosaicism in Fanconi anemia: natural gene therapy via molecular self-correction. 12697994 2002
Fanconi Anemia
CUI: C0015625
Disease: Fanconi Anemia
0.700 CausalMutation CLINVAR Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene. 10094191 1999