ClinVar Miner

Submissions for variant NM_017662.4(TRPM6):c.-167A>C

gnomAD frequency: 0.02299  dbSNP: rs77048628
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000329903 SCV000480728 likely benign Intestinal hypomagnesemia 1 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001672735 SCV001888738 benign not provided 2020-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672735 SCV005226493 likely benign not provided criteria provided, single submitter not provided

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