ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*992G>T

gnomAD frequency: 0.00001  dbSNP: rs886061976
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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 RCV000337688 SCV000466651 uncertain significance Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000396673 SCV000466652 uncertain significance Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing

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