ClinVar Miner

Submissions for variant NM_002472.3(MYH8):c.5166+178G>C

gnomAD frequency: 0.09336  dbSNP: rs79639152
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001710775 SCV001938403 benign not provided 2019-11-02 criteria provided, single submitter clinical testing

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