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Variant (rsID / SNP)

rs6032

F5

rs6032 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F5. Location: chromosome 1, position 169,511,555. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

F5Benign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
1:169511555
Cytoband
1q24.2
HGVS
NM_000130.5(F5):c.2773A>G (p.Lys925Glu)
Allele change
Missense_K925E

Associated conditions / phenotypes

Budd-Chiari syndrome|Factor V deficiency|Thrombophilia due to activated protein C resistance|Thrombophilia due to thrombin defect

Public references

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