Variant (rsID / SNP)
rs5629
rs5629 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTGIS. Location: chromosome 20, position 48,129,706. The table records no clinical significance for this variant.
Reference-table entries
PTGISNot classified
- Variant type
- synonymous_variant
- Chromosome / position
- 20:48129706
- HGVS
- NM_000961.4,c.1117C>A,p.Arg373Arg
- Allele change
- Synonymous_R373R
Associated conditions / phenotypes
Myocardial Infarction
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.