Variant: rs121912625 

    present in Gene: TRPM6
    present in Chromosome: 9
    Position on Chromosome: 74840146
    Alleles of this Variant: G/A

rs121912625 in TRPM6 gene and Hypomagnesemia 1, Intestinal PMID 14976260 2004 Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia.

PMID 12032568 2002 Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family.

PMID 23942199 2014 New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia.