ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.1496G>A (p.Arg499Gln)

dbSNP: rs782243346
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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 RCV001370987 SCV001567537 likely benign Intellectual disability, X-linked 1 2023-08-18 criteria provided, single submitter clinical testing

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