ClinVar Miner

Submissions for variant NM_019026.6(TMCO1):c.-66T>C

gnomAD frequency: 0.00372  dbSNP: rs62622803
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000913229 SCV001058372 benign not provided 2023-08-11 criteria provided, single submitter clinical testing
GeneDx RCV000913229 SCV002546610 likely benign not provided 2021-09-23 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
CeGaT Center for Human Genetics Tuebingen RCV000913229 SCV004126254 benign not provided 2022-08-01 criteria provided, single submitter clinical testing TMCO1: BP4, BS1, BS2

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