ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*2819_*2822dup

dbSNP: rs56247456
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000380489 SCV000466703 uncertain significance Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000265230 SCV000466704 uncertain significance Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004696000 SCV005195638 uncertain significance not provided criteria provided, single submitter not provided

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