Variant: rs104894481 

    present in Gene: PATL2;B2M
    present in Chromosome: 15
    Position on Chromosome: 44711577
    Alleles of this Variant: G/C;T

rs104894481 in PATL2;B2M gene and Hypoproteinemia, Hypercatabolic PMID 16549777 2006 Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene.