"Centre for Mendelian Genomics, University Medical Centre Ljubljana"[s - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 374036	NC_000003.12:g.10133799_10141895del	LOC107303339, VHL	Deletion	Pancreatic cysts +1 more	GPathogenic
Select item 135406	NM_000551.4(VHL):c.3G>A (p.Met1Ile)	VHL (M1I)	Single nucleotide variant (missense variant +1 more)	Von Hippel-Lindau syndrome +6 more	GConflicting classifications of pathogenicity
Select item 182975	NM_000551.4(VHL):c.194C>T (p.Ser65Leu)	VHL (S65L)	Single nucleotide variant (missense variant)	Pancreatic cysts +5 more	GPathogenic

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