Variant (rsID / SNP)

rs3093253

rs3093253 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F10, F7. Location: chromosome 13, position 113,774,092. Clinical significance in the table: Benign.

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Reference-table entries

F10Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 13:113774092
Cytoband: 13q34
HGVS: NM_019616.4(F7):c.*770G>A
Allele change: Silent

Associated conditions / phenotypes

Factor X deficiency|Factor VII deficiency

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.