Variant (rsID / SNP)
rs1799963
rs1799963 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F2. Location: chromosome 11, position 46,761,055. Clinical significance in the table: Conflicting interpretations of pathogenicity; risk factor.
Reference-table entries
F2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity; risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:46761055
- Cytoband
- 11p11.2
- HGVS
- NM_000506.5(F2):c.*97G>A
- Allele change
- Silent
Associated conditions / phenotypes
Thrombophilia due to thrombin defect|Ischemic stroke|Pregnancy loss, recurrent, susceptibility to, 2|Congenital prothrombin deficiency|Venous thromboembolism|Hereditary factor II deficiency disease|Cerebral palsy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.