ClinVar Miner

Submissions for variant NM_022773.4(LMF1):c.1416+13C>T

dbSNP: rs114354808
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001554975 SCV001776319 likely benign not provided 2019-04-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001554975 SCV002473171 benign not provided 2025-01-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001554975 SCV005216376 likely benign not provided criteria provided, single submitter not provided

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