Variant (rsID / SNP)

rs864321642

rs864321642 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,191,516. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

VHLLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:10191516
Cytoband: 3p25.3
HGVS: NM_000551.4(VHL):c.509T>C (p.Val170Ala)
Allele change: Missense_V129A

Associated conditions / phenotypes

Pheochromocytoma

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.