Variant (rsID / SNP)

rs150190385

rs150190385 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F9. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

F9Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xq27.1
HGVS: NM_000133.4(F9):c.19A>T (p.Ile7Phe)
Allele change: Missense_I7F

Associated conditions / phenotypes

Hereditary factor IX deficiency disease|Hereditary factor IX deficiency disease|Thrombophilia, X-linked, due to factor 9 defect|FACTOR IX POLYMORPHISM

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.