ClinVar Miner

Submissions for variant NM_002472.3(MYH8):c.2432+6A>C

gnomAD frequency: 0.00351  dbSNP: rs111692916
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
Genetic Services Laboratory, University of Chicago RCV000192653 SCV000248118 likely benign not specified 2015-06-02 criteria provided, single submitter clinical testing
Invitae RCV000963153 SCV001110290 benign not provided 2018-10-24 criteria provided, single submitter clinical testing

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