ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.4441+8G>A

dbSNP: rs766743441
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000263824 SCV000336214 uncertain significance not provided 2015-10-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000263824 SCV001675693 likely benign not provided 2024-02-01 criteria provided, single submitter clinical testing

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