Variant (rsID / SNP)

rs5898

rs5898 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F2. Location: chromosome 11, position 46,749,648. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

F2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 11:46749648
Cytoband: 11p11.2
HGVS: NM_000506.5(F2):c.1233G>A (p.Pro411=)
Allele change: Synonymous_P395P

Associated conditions / phenotypes

Thrombophilia due to thrombin defect|Congenital prothrombin deficiency

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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