ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*204C>T

gnomAD frequency: 0.00283  dbSNP: rs113405088
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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 RCV000356583 SCV000466637 uncertain significance Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000259341 SCV000466638 uncertain significance Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing

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