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

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.499C>T (p.Arg167Trp)	rs5030820	0.00001
NM_000551.4(VHL):c.473T>A (p.Leu158Gln)	rs121913346
NM_000551.4(VHL):c.481C>T (p.Arg161Ter)	rs5030818

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