Variant (rsID / SNP)
rs1799808
rs1799808 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PROC. Location: chromosome 2, position 128,175,862. The table records no clinical significance for this variant.
Reference-table entries
PROCNot classified
- Variant type
- upstream_gene_variant
- Chromosome / position
- 2:128175862
- HGVS
- NM_001375607.1,c.-161C>T
Associated conditions / phenotypes
Thrombophilia|Pik3ca-Related Overgrowth Syndrome|Protein C Deficiency|Atherosclerosis Susceptibility
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.