Variant (rsID / SNP)
rs149088047
rs149088047 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to F13B. Location: chromosome 1, position 197,020,022. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
F13BConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:197020022
- Cytoband
- 1q31.3
- HGVS
- NM_001994.3(F13B):c.1556-13C>A
- Allele change
- Silent
Associated conditions / phenotypes
Factor XIII, b subunit, deficiency of
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.