List of variants in gene VHL reported as likely benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.74C>T (p.Pro25Leu)	rs35460768	0.00261
NM_000551.4(VHL):c.150C>G (p.Ala50=)	rs61751580	0.00070
NM_000551.4(VHL):c.183C>G (p.Pro61=)	rs63650860	0.00067
NM_000551.4(VHL):c.246C>T (p.Arg82=)	rs587780993	0.00014
NM_000551.4(VHL):c.-47C>T	rs745439844	0.00006
NM_000551.4(VHL):c.340+20G>A	rs757151154	0.00003
NM_000551.4(VHL):c.315G>C (p.Thr105=)	rs769102979	0.00002
NM_000551.4(VHL):c.-35G>A	rs587780992	0.00001
NM_000551.4(VHL):c.123_137dup (p.38SGPEE[3])	rs863224839
NM_000551.4(VHL):c.132C>G (p.Gly44=)	rs1696123413

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