ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.1369C>T (p.Leu457=)

dbSNP: rs769398784
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000983174 SCV001131194 likely benign not provided 2021-07-14 criteria provided, single submitter clinical testing

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