ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.3924G>A (p.Pro1308=)

dbSNP: rs1460397663
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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 RCV000937029 SCV001082803 likely benign Intellectual disability, X-linked 1 2025-01-27 criteria provided, single submitter clinical testing

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