ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.13938A>G (p.Pro4646=)

gnomAD frequency: 0.00001  dbSNP: rs1657802510
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 RCV002119514 SCV002394561 likely benign not provided 2020-12-14 criteria provided, single submitter clinical testing

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