rs1302083447, FANCA

N. diseases: 2
Disease: Fanconi Anemia ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fanconi Anemia
CUI: C0015625
Disease: Fanconi Anemia
0.700 CausalMutation CLINVAR Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia. 29269525 2018