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Variant (rsID / SNP)

rs193922611

VHL

rs193922611 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to VHL. Location: chromosome 3, position 10,188,315. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

VHLConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:10188315
Cytoband
3p25.3
HGVS
NM_000551.4(VHL):c.458T>A (p.Leu153Gln)
Allele change
Silent

Associated conditions / phenotypes

Von Hippel-Lindau syndrome|Hereditary cancer-predisposing syndrome

Public references

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