Variant (rsID / SNP)
rs5051
rs5051 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AGT. Location: chromosome 1, position 230,849,872. Clinical significance in the table: Benign.
Reference-table entries
AGTBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:230849872
- Cytoband
- 1q42.2
- HGVS
- NM_001382817.3(AGT):c.-30-3273G>A
- Allele change
- Silent
Associated conditions / phenotypes
Renal tubular dysgenesis|Hypertension, essential, susceptibility to|Crohn disease, association with
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.