ClinVar Miner

Submissions for variant NM_000257.4(MYH7):c.1579-47C>T

gnomAD frequency: 0.00208  dbSNP: rs45525037
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
PreventionGenetics, part of Exact Sciences RCV000246484 SCV000303210 likely benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001707569 SCV001935774 benign not provided 2019-11-22 criteria provided, single submitter clinical testing

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