List of variants in gene combination LOC107303340, VHL reported as pathogenic for adenocarcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.598C>T (p.Arg200Trp)	rs28940298	0.00010
NM_000551.4(VHL):c.499C>T (p.Arg167Trp)	rs5030820	0.00001
NM_000551.4(VHL):c.464-2A>G	rs5030816
NM_000551.4(VHL):c.482G>A (p.Arg161Gln)	rs730882035
NM_000551.4(VHL):c.506_509delinsCG (p.Leu169fs)
NM_000551.4(VHL):c.530_536del (p.Arg177fs)	rs1575932266
NM_000551.4(VHL):c.548C>A (p.Ser183Ter)	rs5030823

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