Variant (rsID / SNP)
rs59633688
rs59633688 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PCARE. Location: chromosome 2, position 29,286,509. Clinical significance in the table: Benign.
Reference-table entries
PCAREBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:29286509
- Cytoband
- 2p23.2
- HGVS
- NM_001029883.3(PCARE):c.*1226A>G
- 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.