Variant: rs121908022 

    present in Gene: ALG9
    present in Chromosome: 11
    Position on Chromosome: 111836179
    Alleles of this Variant: C/T

rs121908022 in ALG9 gene and Congenital disorder of glycosylation type 1L PMID 15945070 2005 CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features.

PMID 15148656 2004 Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.