"3billion"[submitter] AND "HNF1B"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333532	NM_000458.4(HNF1B):c.1390G>C (p.Gly464Arg)	HNF1B (G438R +1 more)	Single nucleotide variant (missense variant +1 more)	Renal cysts and diabetes syndrome	GUncertain significance
Select item 2444128	NM_000458.4(HNF1B):c.1169A>G (p.Asp390Gly)	HNF1B (D364G +1 more)	Single nucleotide variant (missense variant)	Renal cysts and diabetes syndrome	GUncertain significance
Select item 1333507	NM_000458.4(HNF1B):c.1001C>T (p.Ser334Phe)	HNF1B (S308F +1 more)	Single nucleotide variant (missense variant)	Renal cysts and diabetes syndrome	GUncertain significance
Select item 635638	NM_000458.4(HNF1B):c.840del (p.Ser281fs)	HNF1B (S255fs +1 more)	Deletion (frameshift variant)	Renal cysts and diabetes syndrome	GPathogenic
Select item 12643	NM_000458.4(HNF1B):c.544+1G>A	HNF1B	Single nucleotide variant (splice donor variant)	Type 2 diabetes mellitus +3 more	GPathogenic
Select item 586800	NM_000458.4(HNF1B):c.473C>A (p.Thr158Asn)	HNF1B (T158N)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1526083	NM_000458.4(HNF1B):c.410G>A (p.Arg137Lys)	HNF1B (R137K)	Single nucleotide variant (missense variant)	Type 2 diabetes mellitus	GUncertain significance

ClinVar