Variant (rsID / SNP)

rs137852240

rs137852240 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F9. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

F9Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xq27.1
HGVS: NM_000133.4(F9):c.676C>T (p.Arg226Trp)
Allele change: Missense_R188W

Associated conditions / phenotypes

Hereditary factor IX deficiency disease

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.