ClinVar for PubMed (Select 16809612) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 428809	NM_000551.4(VHL):c.506T>C (p.Leu169Pro)	LOC107303340, VHL (L169P +1 more)	Single nucleotide variant (missense variant +1 more)	Chuvash polycythemia +2 more	GConflicting classifications of pathogenicity
Select item 428803	NM_000551.4(VHL):c.452T>C (p.Ile151Thr)	LOC107303340, VHL (I151T)	Single nucleotide variant (missense variant +1 more)	Von Hippel-Lindau syndrome +3 more	GPathogenic