ClinVar Miner

Submissions for variant NM_017662.5(TRPM6):c.5083+53C>T

gnomAD frequency: 0.02546  dbSNP: rs73650058
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001612554 SCV001842308 benign not provided 2020-05-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001612554 SCV005266305 benign not provided criteria provided, single submitter not provided

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