ClinVar Miner

Submissions for variant NM_017662.5(TRPM6):c.2667+1G>A

dbSNP: rs869025214
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pediatric Genetics Division, Center for Pediatrics and Adolescent Medicine, University Medical Center Freiburg RCV000207483 SCV000257394 pathogenic Intestinal hypomagnesemia 1 2013-09-01 criteria provided, single submitter research
OMIM RCV000207483 SCV000023924 pathogenic Intestinal hypomagnesemia 1 2002-06-01 no assertion criteria provided literature only

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