Variant (rsID / SNP)

rs5960

rs5960 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F10. Location: chromosome 13, position 113,801,737. 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: 13:113801737
Cytoband: 13q34
HGVS: NM_000504.4(F10):c.792C>T (p.Thr264=)
Allele change: Synonymous_T264T

Associated conditions / phenotypes

Hereditary factor X 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.