ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.999C>T (p.Pro333=)

gnomAD frequency: 0.00002  dbSNP: rs192630206
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
Eurofins Ntd Llc (ga) RCV000311399 SCV000344556 uncertain significance not provided 2016-09-01 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000311399 SCV004537438 likely benign not provided 2024-03-17 criteria provided, single submitter clinical testing

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