ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.10941T>C (p.Gly3647=)

gnomAD frequency: 0.00004  dbSNP: rs563945220
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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 RCV001424556 SCV001627154 likely benign not provided 2024-03-12 criteria provided, single submitter clinical testing

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