Variant (rsID / SNP)

rs151202877

rs151202877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F8. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

F8Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_000132.4(F8):c.5303G>A (p.Arg1768His)
Allele change: Missense_R1768H

Associated conditions / phenotypes

Abnormal bleeding

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.