Variant (rsID / SNP)
rs4147843
rs4147843 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA4. Location: chromosome 1, position 94,495,816. Clinical significance in the table: Benign.
Reference-table entries
ABCA4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:94495816
- Cytoband
- 1p22.1
- HGVS
- NM_000350.3(ABCA4):c.4352+168A>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.