ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.8347G>A (p.Val2783Met)

gnomAD frequency: 0.00023  dbSNP: rs201214320
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
Athena Diagnostics RCV000712350 SCV000842824 uncertain significance not provided 2018-05-25 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000712350 SCV003484697 benign not provided 2023-12-09 criteria provided, single submitter clinical testing

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