Variant (rsID / SNP)
rs2067853
rs2067853 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGT. Location: chromosome 1, position 230,838,258. Clinical significance in the table: Benign.
Reference-table entries
AGTBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:230838258
- Cytoband
- 1q42.2
- HGVS
- NM_000029.3(AGT):c.*629C>T
Associated conditions / phenotypes
Renal tubular dysgenesis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.