ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.5327-10C>T

gnomAD frequency: 0.00002  dbSNP: rs781062618
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV001289030 SCV001476554 uncertain significance not provided 2019-09-30 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001289030 SCV001596733 likely benign not provided 2024-02-19 criteria provided, single submitter clinical testing

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