ClinVar Miner

Submissions for variant NM_031844.3(HNRNPU):c.423G>T (p.Gly141=)

dbSNP: rs777752880
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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 RCV002564021 SCV001415296 likely benign Developmental and epileptic encephalopathy, 54 2025-01-28 criteria provided, single submitter clinical testing

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