ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.9276A>C (p.Ile3092=)

gnomAD frequency: 0.00001  dbSNP: rs757205145
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001873989 SCV002118186 likely benign not provided 2024-01-18 criteria provided, single submitter clinical testing

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