List of variants in gene VHL reported as pathogenic for benign neoplasm

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.188T>C (p.Leu63Pro)	rs104893827
NM_000551.4(VHL):c.191G>C (p.Arg64Pro)	rs104893826
NM_000551.4(VHL):c.194C>T (p.Ser65Leu)	rs5030826
NM_000551.4(VHL):c.277G>A (p.Gly93Ser)	rs5030808

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