ClinVar Miner

Submissions for variant NM_198271.5(LMOD3):c.788T>C (p.Ile263Thr)

dbSNP: rs9835034
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000544001 SCV000655518 likely benign Nemaline myopathy 10 2025-01-23 criteria provided, single submitter clinical testing
Baylor Genetics RCV000544001 SCV001527667 uncertain significance Nemaline myopathy 10 2018-02-21 criteria provided, single submitter clinical testing This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].
GeneDx RCV001562953 SCV001785806 likely benign not provided 2020-03-06 criteria provided, single submitter clinical testing

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