Variant (rsID / SNP)
rs11601325
rs11601325 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CABP4. Location: chromosome 11, position 67,227,006. Clinical significance in the table: Benign.
Reference-table entries
CABP4Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 11:67227006
- Cytoband
- 11q13.2
- HGVS
- NM_145200.5(CABP4):c.*876G>A
- Allele change
- Silent
Associated conditions / phenotypes
Cone-rod synaptic disorder, congenital nonprogressive
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.