Variant: rs104893987 

    present in Gene: RHAG
    present in Chromosome: 6
    Position on Chromosome: 49612504
    Alleles of this Variant: C/T

rs104893987 in RHAG gene and Rh-Null, Regulator Type PMID 8563755 1996 Candidate gene acting as a suppressor of the RH locus in most cases of Rh-deficiency.

PMID 9454778 1998 A novel single missense mutation identified along the RH50 gene in a composite heterozygous Rhnull blood donor of the regulator type.

PMID 9716608 1998 Rh50 glycoprotein gene and rhnull disease: a silent splice donor is trans to a Gly279-->Glu missense mutation in the conserved transmembrane segment.

PMID 10467273 1999 Molecular basis for Rh(null) syndrome: identification of three new missense mutations in the Rh50 glycoprotein gene.