Variant (rsID / SNP)
rs1474867
rs1474867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GUCA1B. Location: chromosome 6, position 42,162,575. Clinical significance in the table: Benign.
Reference-table entries
GUCA1BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:42162575
- Cytoband
- 6p21.1
- HGVS
- NM_002098.6(GUCA1B):c.-17T>C
- Allele change
- Silent
Associated conditions / phenotypes
Retinitis pigmentosa 48
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.