Variant (rsID / SNP)
rs593421
rs593421 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4F12. Location: chromosome 19, position 15,807,830. The table records no clinical significance for this variant.
Reference-table entries
CYP4F12Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 19:15807830
- HGVS
- NM_023944.4,c.1510T>C,p.Leu504Leu
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.