ClinVar Miner

Submissions for variant NM_175914.5(HNF4A):c.609C>T (p.Gly203=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003736386 SCV004563358 likely benign not provided 2023-09-12 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005038505 SCV005656977 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 2024-03-13 criteria provided, single submitter clinical testing

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