ClinVar Miner

Submissions for variant NM_004998.4(MYO1E):c.1617-16_1617-15del

dbSNP: rs146306690
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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
Labcorp Genetics (formerly Invitae), Labcorp RCV001522827 SCV001732439 benign not provided 2024-01-06 criteria provided, single submitter clinical testing
GeneDx RCV001522827 SCV001826542 likely benign not provided 2020-10-29 criteria provided, single submitter clinical testing

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