Variant (rsID / SNP)

rs137852402

rs137852402 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F8. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

F8Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000132.4(F8):c.896A>T (p.Asn299Ile)
Allele change: Missense_N299I

Associated conditions / phenotypes

Hereditary factor VIII 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.