Variant (rsID / SNP)
rs4524
rs4524 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F5. Location: chromosome 1, position 169,511,755. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
F5Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:169511755
- Cytoband
- 1q24.2
- HGVS
- NM_000130.5(F5):c.2573A>G (p.Lys858Arg)
- Allele change
- Missense_K858R
Associated conditions / phenotypes
Thrombophilia due to activated protein C resistance
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.