Variant (rsID / SNP)
rs2815736
rs2815736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RIMS1. Location: chromosome 6, position 73,111,454. Clinical significance in the table: Benign.
Reference-table entries
RIMS1Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 6:73111454
- Cytoband
- 6q13
- HGVS
- NM_014989.7(RIMS1):c.*1038A>G
- Allele change
- Silent
Associated conditions / phenotypes
Cone-rod dystrophy 7
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.