Variant (rsID / SNP)
rs1352275281
rs1352275281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,191,499. Clinical significance in the table: Pathogenic.
Reference-table entries
VHLPathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:10191499
- Cytoband
- 3p25.3
- HGVS
- NM_000551.4(VHL):c.492G>T (p.Gln164His)
- Allele change
- Missense_Q123H
Associated conditions / phenotypes
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.