Variant (rsID / SNP)
rs61752390
rs61752390 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,546,047. The table records no clinical significance for this variant.
Reference-table entries
ABCA4Not classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:94546047
- Cytoband
- 1p22.1
- HGVS
- NM_000350.3(ABCA4):c.1086T>G (p.Tyr362Ter)
- Allele change
- Nonsense_Y362X
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.