List of variants in gene VHL reported as likely pathogenic by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.242C>T (p.Pro81Leu)	rs193922608	0.00001
NM_000551.4(VHL):c.189dup (p.Arg64fs)	rs1553619402
NM_000551.4(VHL):c.192del (p.Ser65fs)	rs730882031
NM_000551.4(VHL):c.245G>T (p.Arg82Leu)	rs794726890
NM_000551.4(VHL):c.256C>G (p.Pro86Ala)	rs398123481
NM_000551.4(VHL):c.336C>G (p.Tyr112Ter)	rs751232153
NM_000551.4(VHL):c.340+1G>C	rs730882032
p.X214Trp

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