ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.322G>A (p.Ala108Thr)

dbSNP: rs1358951592
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001330294 SCV001521935 uncertain significance Noonan syndrome 10 2019-04-03 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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