Variant (rsID / SNP)
rs1799809
rs1799809 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROC. Location: chromosome 2, position 128,175,875. The table records no clinical significance for this variant.
Reference-table entries
PROCNot classified
- Variant type
- upstream_gene_variant
- Chromosome / position
- 2:128175875
- HGVS
- NM_001375607.1,c.-148G>A
Associated conditions / phenotypes
Atherosclerosis Susceptibility|Stroke, Ischemic|Pulmonary Embolism
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.