Variant (rsID / SNP)
rs55896821
rs55896821 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,505,711. The table records no clinical significance for this variant.
Reference-table entries
ABCA4Not classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:94505711
- Cytoband
- 1p22.1
- HGVS
- NM_000350.3(ABCA4):c.3523-28T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
