Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912625
rs121912625
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia. 23942199

2014
dbSNP: rs121912625
rs121912625
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia. 14976260

2004
dbSNP: rs121912625
rs121912625
TRPM6
CUI: C1865974
Disease: Hypomagnesemia 1, Intestinal
Hypomagnesemia 1, Intestinal 		0.800 GeneticVariation UNIPROT Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family. 12032568

2002
dbSNP: rs1193127627
rs1193127627
TRPM6
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		0.700 GeneticVariation UNIPROT