ClinVar Miner

Submissions for variant NM_001709.5(BDNF):c.557G>A (p.Cys186Tyr)

dbSNP: rs1852795747
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Goettingen RCV001261409 SCV001438331 likely pathogenic Obesity 2020-10-13 criteria provided, single submitter clinical testing ACMG criteria used for classification: PS2, PM2, PP3, BP1.

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