"Mendelics"[submitter] AND "HNF1B"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1684798	NM_000458.4(HNF1B):c.1441C>G (p.Pro481Ala)	HNF1B (P455A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 594776	NM_000458.4(HNF1B):c.254A>G (p.Asp85Gly)	HNF1B (D85G)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1685245	NM_000458.4(HNF1B):c.-35A>C	HNF1B	Single nucleotide variant (5 prime UTR variant)	not specified	GBenign

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