ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.6559-43T>C

dbSNP: rs112028203
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 RCV001651710 SCV001862133 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001651710 SCV005235711 benign not provided criteria provided, single submitter not provided

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