Variants in gene VHL with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000551.4(VHL):c.189dup (p.Arg64fs)	rs1553619402
NM_000551.4(VHL):c.191G>C (p.Arg64Pro)	rs104893826
NM_000551.4(VHL):c.208G>A (p.Glu70Lys)	rs5030802
NM_000551.4(VHL):c.224TCT[1] (p.Phe76del)	rs5030648
NM_000551.4(VHL):c.232A>G (p.Asn78Asp)	rs869025621
NM_000551.4(VHL):c.239G>T (p.Ser80Ile)	rs5030805
NM_000551.4(VHL):c.256C>T (p.Pro86Ser)	rs398123481
NM_000551.4(VHL):c.257C>G (p.Pro86Arg)	rs730882034
NM_000551.4(VHL):c.257C>T (p.Pro86Leu)	rs730882034
NM_000551.4(VHL):c.293A>G (p.Tyr98Cys)	rs864321643

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.