ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.6958-10A>G

gnomAD frequency: 0.00001  dbSNP: rs727504213
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000154110 SCV000203773 uncertain significance not provided 2014-04-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000154110 SCV001701527 likely benign not provided 2024-01-14 criteria provided, single submitter clinical testing

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