ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.-52+175C>T

gnomAD frequency: 0.39124  dbSNP: rs225320
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001708655 SCV001935937 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001708655 SCV005310725 benign not provided criteria provided, single submitter not provided

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