Variant: rs757863670 

    present in Gene: B9D2
    present in Chromosome: 19
    Position on Chromosome: 41358004
    Alleles of this Variant: A/G

rs757863670 in B9D2 gene and Familial aplasia of the vermis PMID 26092869 2015 Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.

rs757863670 in B9D2 gene and MECKEL SYNDROME, TYPE 10 PMID 26092869 2015 Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.