ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.3285+91dup

dbSNP: rs112227803
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 RCV001725692 SCV001960696 benign not provided 2018-07-23 criteria provided, single submitter clinical testing

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