ClinVar Miner

Submissions for variant NM_001174147.2(LMX1B):c.924del (p.Tyr309fs)

dbSNP: rs1588309277
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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, Cologne University RCV000857318 SCV000999914 likely pathogenic Nail-patella syndrome no assertion criteria provided clinical testing

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