ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.2904+142G>A

gnomAD frequency: 0.05866  dbSNP: rs56333771
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 RCV001617179 SCV001846506 benign not provided 2018-07-09 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001617179 SCV005236384 benign not provided criteria provided, single submitter not provided

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