Variant (rsID / SNP)
rs4646450
rs4646450 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP3A5, ZSCAN25. Location: chromosome 7, position 99,266,318. Clinical significance in the table: association.
Reference-table entries
CYP3A5Association
- Clinical significance (as recorded)
- association
- Variant type
- single nucleotide variant
- Chromosome / position
- 7:99266318
- Cytoband
- 7q22.1
- HGVS
- NM_000777.5(CYP3A5):c.319-1630C>T
- Allele change
- Silent
Associated conditions / phenotypes
appendicular lean mass relative to body height
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.