ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.3729C>G (p.Pro1243=)

dbSNP: rs1277398294
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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 RCV001448652 SCV001651748 likely benign not provided 2020-09-01 criteria provided, single submitter clinical testing

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