ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*2820_*2822dup

dbSNP: rs56247456
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000261284 SCV000466701 likely benign Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000323539 SCV000466702 likely benign Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing

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