Variant (rsID / SNP)
rs609290
rs609290 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP4F12. Location: chromosome 19, position 15,789,140. The table records no clinical significance for this variant.
Reference-table entries
CYP4F12Not classified
- Variant type
- splice_donor_variant&intron_variant
- Chromosome / position
- 19:15789140
- HGVS
- NR_117085.2,n.317+1A>G
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.