ClinVar Miner

Submissions for variant NM_000525.4(KCNJ11):c.99C>T (p.Ala33=)

dbSNP: rs1489389760
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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 RCV001463240 SCV001667178 likely benign not provided 2021-10-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002501611 SCV002805426 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 2021-07-19 criteria provided, single submitter clinical testing

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