Variant (rsID / SNP)
rs186571865
rs186571865 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RP1. Location: chromosome 8, position 55,534,671. Clinical significance in the table: Benign.
Reference-table entries
RP1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 8:55534671
- Cytoband
- 8q12.1
- HGVS
- NM_006269.2(RP1):c.616-6T>C
- 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.