ClinVar Miner

Submissions for variant NM_000230.3(LEP):c.*1720A>G

dbSNP: rs10954174
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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 RCV000404055 SCV000466669 benign Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000279850 SCV000466670 benign Obesity due to congenital leptin deficiency 2016-06-14 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004712337 SCV005267145 benign not provided criteria provided, single submitter not provided

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