Variant (rsID / SNP)
rs121909603
rs121909603 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CD55. Location: chromosome 1, position 207,495,887. Clinical significance in the table: Pathogenic.
Reference-table entries
CD55Pathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:207495887
- Cytoband
- 1q32.2
- HGVS
- NM_000574.5(CD55):c.261G>A (p.Trp87Ter)
- Allele change
- Nonsense_W87X
Associated conditions / phenotypes
Cromer blood group system
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.