Variant (rsID / SNP)
rs8176746
rs8176746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,131,322. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- missense_variant
- Chromosome / position
- 9:136131322
- HGVS
- NM_020469.3,c.793C>A,p.Leu265Met
- Allele change
- Synonymous_T265T
Associated conditions / phenotypes
Malaria|Plasmodium Falciparum Malaria|Pancreatic Cancer|Helicobacter Pylori Infection|Hypercholesterolemia, Familial, 1|Hypertension, Essential|Prostate Cancer|Adult Respiratory Distress Syndrome|Heart Disease|Thrombosis|Familial Hypercholesterolemia|Mental Depression|Hypercholesterolemia, Familial, 3|Major Depressive Disorder|Gastric Cancer|Microcephaly 1, Primary, Autosomal Recessive|Enterocolitis|Autoinflammation with Infantile Enterocolitis
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.