ClinVar Miner

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

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Total variants: 6
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HGVS dbSNP
NM_000551.3(VHL):c.233A>T (p.Asn78Ile) rs5030804
NM_000551.3(VHL):c.242C>T (p.Pro81Leu) rs193922608
NM_000551.3(VHL):c.264G>T (p.Trp88Cys) rs869025622
NM_000551.3(VHL):c.331A>G (p.Ser111Gly) rs1559426203
NM_000551.3(VHL):c.335A>G (p.Tyr112Cys) rs869025633
NM_000551.4(VHL):c.160A>T (p.Met54Leu)

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