Variant (rsID / SNP)

rs137852459

rs137852459 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F8. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

F8Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000132.4(F8):c.6371A>G (p.Tyr2124Cys)
Allele change: Missense_Y2124C

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.