ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*366A>T

gnomAD frequency: 0.03579  dbSNP: rs28954118
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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 RCV000383918 SCV000466643 uncertain significance Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000292035 SCV000466644 uncertain significance Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004695997 SCV005195635 uncertain significance not provided criteria provided, single submitter not provided

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