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Variant (rsID / SNP)

rs765978945

VHL

rs765978945 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,183,864. Clinical significance in the table: Pathogenic.

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Reference-table entries

VHLPathogenic
Clinical significance (as recorded)
Pathogenic
Variant type
single nucleotide variant
Chromosome / position
3:10183864
Cytoband
3p25.3
HGVS
NM_000551.4(VHL):c.333C>G (p.Ser111Arg)
Allele change
Missense_S111R

Associated conditions / phenotypes

Von Hippel-Lindau syndrome|Hereditary cancer-predisposing 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.