Variant (rsID / SNP)
rs74635192
rs74635192 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRPF8. Location: chromosome 17, position 1,588,141. Clinical significance in the table: Benign.
Reference-table entries
PRPF8Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:1588141
- Cytoband
- 17p13.3
- HGVS
- NM_006445.4(PRPF8):c.-79C>T
- 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.