Variant (rsID / SNP)
rs869025637
rs869025637 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,188,196. Clinical significance in the table: Pathogenic.
Reference-table entries
VHLPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:10188196
- Cytoband
- 3p25.3
- HGVS
- NM_000551.4(VHL):c.341-2A>G
- Allele change
- Silent
Associated conditions / phenotypes
Von Hippel-Lindau syndrome|Von Hippel-Lindau syndrome|Chuvash polycythemia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.