ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.1739T>C (p.Leu580Pro)

dbSNP: rs1555928697
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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 RCV000677201 SCV000803339 uncertain significance Noonan syndrome 10 no assertion criteria provided clinical testing

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