Variant (rsID / SNP)
rs794727253
rs794727253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,188,305. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
VHLPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 3:10188305
- Cytoband
- 3p25.3
- HGVS
- NM_000551.4(VHL):c.449del (p.Asn150fs)
Associated conditions / phenotypes
Von Hippel-Lindau syndrome|Chuvash polycythemia|Von Hippel-Lindau syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.