ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.2078-19T>C

gnomAD frequency: 0.00105  dbSNP: rs188730005
Minimum review status: Collection method:
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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
GeneDx RCV001567910 SCV001791683 likely benign not provided 2019-12-23 criteria provided, single submitter clinical testing
Invitae RCV001567910 SCV002489266 benign not provided 2024-01-07 criteria provided, single submitter clinical testing

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