Variant (rsID / SNP)
rs888895
rs888895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PDE6A. Location: chromosome 5, position 149,239,093. Clinical significance in the table: Benign.
Reference-table entries
PDE6ABenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 5:149239093
- Cytoband
- 5q32
- HGVS
- NM_000440.3(PDE6A):c.*1365G>A
- Allele change
- Silent
Associated conditions / phenotypes
Retinitis pigmentosa
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.