Variant (rsID / SNP)
rs12487736
rs12487736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCAP. Location: chromosome 3, position 47,459,679. The table records no clinical significance for this variant.
Reference-table entries
SCAPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 3:47459679
- HGVS
- NM_012235.4,c.2392G>A,p.Val798Ile
- Allele change
- Missense_V543I
Associated conditions / phenotypes
Lipoprotein Quantitative Trait Locus|Arteries, Anomalies of|Cardiac Conduction Defect|Coronary Stenosis|Lipid Metabolism Disorder
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.