Variant (rsID / SNP)
rs4151672
rs4151672 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CFB. Location: chromosome 6, position 31,919,830. Clinical significance in the table: Benign.
Reference-table entries
CFBBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:31919830
- Cytoband
- 6p21.33
- HGVS
- NM_001710.6(CFB):c.*23C>T
- Allele change
- Silent
Associated conditions / phenotypes
Macular degeneration|Atypical hemolytic-uremic syndrome with B factor anomaly
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.