ClinVar Miner

Submissions for variant NM_002500.5(NEUROD1):c.189T>C (p.Asp63=)

dbSNP: rs2105595687
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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 RCV002178587 SCV002474634 likely benign not provided 2022-01-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500381 SCV002809276 likely benign Maturity-onset diabetes of the young type 6; Type 2 diabetes mellitus 2022-03-28 criteria provided, single submitter clinical testing

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