ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.205+210A>G

gnomAD frequency: 0.09698  dbSNP: rs3814900
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 RCV001657102 SCV001867175 benign not provided 2018-12-21 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001657102 SCV005310719 benign not provided criteria provided, single submitter not provided

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