Variant (rsID / SNP)

rs5896

rs5896 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F2. Location: chromosome 11, position 46,745,003. 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: 11:46745003
Cytoband: 11p11.2
HGVS: NM_000506.5(F2):c.494C>T (p.Thr165Met)
Allele change: Missense_T149M

Associated conditions / phenotypes

Congenital prothrombin deficiency|Thrombophilia due to thrombin defect

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.