ClinVar Miner

Submissions for variant NM_014319.5(LEMD3):c.292C>T (p.Leu98Phe)

gnomAD frequency: 0.00052  dbSNP: rs571742271
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000319423 SCV000337320 uncertain significance not provided 2015-11-18 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000319423 SCV002400585 benign not provided 2023-10-04 criteria provided, single submitter clinical testing

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