Variant (rsID / SNP)
rs288326
rs288326 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FRZB. Location: chromosome 2, position 183,703,336. Clinical significance in the table: risk factor.
Reference-table entries
FRZBRisk factor
- Clinical significance (as recorded)
- risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:183703336
- Cytoband
- 2q32.1
- HGVS
- NM_001463.4(FRZB):c.598C>T (p.Arg200Trp)
- Allele change
- Missense_R200W
Associated conditions / phenotypes
Osteoarthritis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.