FANCG, FA complementation group G, 2189

N. diseases: 132; N. variants: 19
Disease: Fanconi Anemia ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1209807088
rs1209807088
Entrez Id: 2189
Gene Symbol: FANCG
FANCG
CUI: C0015625
Disease:
Fanconi Anemia 		A 0.700 CausalMutation CLINVAR