ClinVar Miner

Submissions for variant NM_003289.4(TPM2):c.375-25C>T

gnomAD frequency: 0.00611  dbSNP: rs41312812
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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
PreventionGenetics, part of Exact Sciences RCV000252343 SCV000309557 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001582853 SCV001820622 likely benign not provided 2018-06-28 criteria provided, single submitter clinical testing

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