ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.3798C>A (p.Ala1266=)

dbSNP: rs2147003811
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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 RCV001431121 SCV001633873 likely benign Intellectual disability, X-linked 1 2024-08-21 criteria provided, single submitter clinical testing

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