Variant (rsID / SNP)
rs9332608
rs9332608 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F5. Location: chromosome 1, position 169,510,118. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
F5Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:169510118
- Cytoband
- 1q24.2
- HGVS
- NM_000130.5(F5):c.4210C>T (p.Pro1404Ser)
- Allele change
- Missense_P1404S
Associated conditions / phenotypes
Thrombophilia due to activated protein C resistance|Factor V deficiency|Thrombophilia due to thrombin defect|Budd-Chiari syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.