Variant (rsID / SNP)
rs1163750
rs1163750 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ROBO2. Location: chromosome 3, position 77,698,442. Clinical significance in the table: Benign.
Reference-table entries
ROBO2Benign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:77698442
- Cytoband
- 3p12.3
- HGVS
- NM_001395656.1(ROBO2):c.*3236G>A
- Allele change
- Silent
Associated conditions / phenotypes
Vesicoureteral reflux 2
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.