ClinVar Miner

Submissions for variant NM_175914.5(HNF4A):c.463C>G (p.Arg155Gly)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005028912 SCV005656972 uncertain significance Maturity-onset diabetes of the young type 1; Type 2 diabetes mellitus; Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young 2024-05-18 criteria provided, single submitter clinical testing

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