ClinVar Miner

Submissions for variant NM_002303.6(LEPR):c.*188A>C

dbSNP: rs886046507
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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 RCV000282446 SCV000358843 uncertain significance Obesity due to leptin receptor gene deficiency 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000318844 SCV000358844 uncertain significance Monogenic Non-Syndromic Obesity 2016-06-14 criteria provided, single submitter clinical testing

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