"Broad Center for Mendelian Genomics, Broad Institute of MIT and Harva - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 972765	NM_000545.8(HNF1A):c.1849G>A (p.Val617Ile)	C12orf43, HNF1A (V617I +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Monogenic diabetes	GBenign FDA Recognized database
Select item 972764	NM_000545.8(HNF1A):c.1855G>A (p.Glu619Lys)	C12orf43, HNF1A (E619K +1 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Maturity-onset diabetes of the young type 3 +2 more	GConflicting classifications of pathogenicity