Variant: rs1569083185 

    present in Gene: FANCB
    present in Chromosome: X
    Position on Chromosome: 14844518
    Alleles of this Variant: A/C

rs1569083185 in FANCB gene and FANCONI ANEMIA, COMPLEMENTATION GROUP B PMID 21910217 2011 X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.