ClinVar Miner

Submissions for variant NM_015374.3(SUN2):c.2074C>T (p.Leu692=)

dbSNP: rs1603210228
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001444978 SCV001647996 likely benign Emery-Dreifuss muscular dystrophy 2018-12-24 criteria provided, single submitter clinical testing

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