Variant (rsID / SNP)
rs9826147
rs9826147 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FLNB. Location: chromosome 3, position 58,129,450. Clinical significance in the table: Benign.
Reference-table entries
FLNBBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:58129450
- Cytoband
- 3p14.3
- HGVS
- NM_001457.4(FLNB):c.5425+110A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.