ClinVar Miner

Submissions for variant NM_000525.4(KCNJ11):c.66_67inv (p.Lys23Glu)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001434167 SCV001636970 likely benign not provided 2024-01-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501532 SCV002808989 likely benign Diabetes mellitus, transient neonatal, 3; Hyperinsulinemic hypoglycemia, familial, 2; Type 2 diabetes mellitus; Maturity-onset diabetes of the young type 13; Diabetes mellitus, permanent neonatal 2 2022-05-11 criteria provided, single submitter clinical testing

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