ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.10183-20A>C

gnomAD frequency: 0.00016  dbSNP: rs938186162
Minimum review status: Collection method:
Minimum conflict level:
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 RCV002095184 SCV002382176 likely benign not provided 2024-06-30 criteria provided, single submitter clinical testing

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