ClinVar Miner

Submissions for variant NM_002303.6(LEPR):c.3268_3269dup (p.Ser1090fs)

dbSNP: rs1553174844
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Gujarat Genomics Initiative, Gujarat State Biotechnology Mission RCV000626385 SCV000622177 pathogenic Obesity due to leptin receptor gene deficiency 2016-01-01 no assertion criteria provided research

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