ClinVar Miner

Submissions for variant NM_002303.6(LEPR):c.371-26_371-25insG

gnomAD frequency: 0.00031  dbSNP: rs767256351
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 RCV001576634 SCV001803863 likely benign not provided 2019-09-11 criteria provided, single submitter clinical testing

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