ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.8157C>T (p.His2719=)

gnomAD frequency: 0.00067  dbSNP: rs373955726
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000594983 SCV000703592 uncertain significance not provided 2016-12-06 criteria provided, single submitter clinical testing
GeneDx RCV000594983 SCV001813498 likely benign not provided 2020-10-06 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000594983 SCV002461329 benign not provided 2023-12-26 criteria provided, single submitter clinical testing

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