ClinVar Miner

List of variants in gene combination LOC107303340, VHL reported as likely benign for Erythrocytosis, familial, 2; Von Hippel-Lindau syndrome

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Total variants: 3
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NM_000551.3(VHL):c.402A>G (p.Glu134=) rs201482330
NM_000551.3(VHL):c.411G>C (p.Val137=) rs1553619969
NM_000551.3(VHL):c.504C>T (p.Ser168=) rs1553620323

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