Variant (rsID / SNP)
rs4253865
rs4253865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F11. Location: chromosome 4, position 187,210,090. Clinical significance in the table: Benign.
Reference-table entries
F11Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 4:187210090
- Cytoband
- 4q35.2
- HGVS
- NM_000128.4(F11):c.*322G>A
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary factor XI deficiency disease
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.