Variant (rsID / SNP)
rs34433079
rs34433079 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RD3. Location: chromosome 1, position 211,651,907. Clinical significance in the table: Benign.
Reference-table entries
RD3Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:211651907
- Cytoband
- 1q32.3
- HGVS
- NM_001164688.2(RD3):c.*471C>T
- Allele change
- Silent
Associated conditions / phenotypes
Leber congenital amaurosis 12
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.