FANCB, FA complementation group B, 2187

N. diseases: 278; N. variants: 6
Disease: FANCONI ANEMIA, COMPLEMENTATION GROUP B ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1569083185
rs1569083185
Entrez Id: 2187
Gene Symbol: FANCB
FANCB
CUI: C1845292
Disease:
FANCONI ANEMIA, COMPLEMENTATION GROUP B 		C 0.700 CausalMutation CLINVAR X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations. 21910217 2011