Variant (rsID / SNP)
rs3561
rs3561 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NRL. Location: chromosome 14, position 24,550,224. Clinical significance in the table: Benign.
Reference-table entries
NRLBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 14:24550224
- Cytoband
- 14q11.2
- HGVS
- NM_001354768.3(NRL):c.*221G>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.