Variant (rsID / SNP)
rs28369860
rs28369860 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FMO2. Location: chromosome 1, position 171,165,803. Clinical significance in the table: Benign.
Reference-table entries
FMO2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- Deletion
- Chromosome / position
- 1:171165803
- Cytoband
- 1q24.3
- HGVS
- NM_001460.5(FMO2):c.337del (p.Ser112_Val113insTer)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.