ClinVar Miner

Submissions for variant NM_144672.4(OTOA):c.1320+19C>T

gnomAD frequency: 0.00024  dbSNP: rs199792638
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000241842 SCV000316023 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058404 SCV002408281 benign not provided 2024-11-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002058404 SCV005213457 likely benign not provided criteria provided, single submitter not provided

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