ClinVar Miner

Submissions for variant NM_012335.4(MYO1F):c.2854+193A>C

gnomAD frequency: 0.05934  dbSNP: rs10402716
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
GeneDx RCV001621622 SCV001843445 benign not provided 2021-05-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001621622 SCV005309056 benign not provided criteria provided, single submitter not provided

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