ClinVar Miner

Submissions for variant NM_001256317.3(TMPRSS3):c.1293G>C (p.Gly431=)

gnomAD frequency: 0.00003  dbSNP: rs369050452
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
Athena Diagnostics RCV000993335 SCV001146201 likely benign not provided 2019-07-10 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000993335 SCV004682949 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing

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