ClinVar Miner

Submissions for variant NM_006767.4(LZTR1):c.1449+9C>G

dbSNP: rs756813850
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001510241 SCV001717227 benign not provided 2024-01-04 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV004533920 SCV004719529 likely benign LZTR1-related disorder 2019-08-02 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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