Variant (rsID / SNP)
rs776746
rs776746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP3A5. Location: chromosome 7, position 99,270,539. Clinical significance in the table: association; drug response; risk factor.
Reference-table entries
CYP3A5Drug response
- Clinical significance (as recorded)
- association; drug response; risk factor
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:99270539
- Cytoband
- 7q22.1
- HGVS
- NM_000777.5(CYP3A5):c.219-237A>G
- Allele change
- Silent
Associated conditions / phenotypes
Hypertension, salt-sensitive essential, susceptibility to|refractory myasthenia gravis|Tacrolimus response
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.