ClinVar Miner

List of variants in gene VHL reported as likely benign for Von Hippel-Lindau syndrome

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_000551.3(VHL):c.-77C>T rs3087462
NM_000551.3(VHL):c.114C>T (p.Ser38=) rs417164
NM_000551.3(VHL):c.135G>A (p.Pro45=) rs773519476
NM_000551.3(VHL):c.183C>G (p.Pro61=) rs63650860
NM_000551.3(VHL):c.246C>T (p.Arg82=) rs587780993
NM_000551.3(VHL):c.258C>G (p.Pro86=) rs781063331
NM_000551.3(VHL):c.271T>G (p.Phe91Val) rs1559426039
NM_000551.3(VHL):c.340+7G>C rs869025635
NM_000551.3(VHL):c.340+8C>T rs756068442
NM_000551.4(VHL):c.241C>T (p.Pro81Ser) rs104893829

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