ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.323-8T>C

gnomAD frequency: 0.00006  dbSNP: rs201482591
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
Invitae RCV000921756 SCV001067168 benign not provided 2024-01-19 criteria provided, single submitter clinical testing
GeneDx RCV000921756 SCV001791101 likely benign not provided 2020-03-31 criteria provided, single submitter clinical testing

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