Variant (rsID / SNP)
rs8176719
rs8176719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,132,908. The table records no clinical significance for this variant.
Reference-table entries
- Variant type
- splice_acceptor_variant&splice_donor_variant&intron_variant
- Chromosome / position
- 9:136132908
- HGVS
- NM_020469.3,c.259-1_259insG
Associated conditions / phenotypes
Thrombophilia Due to Thrombin Defect|Thrombosis|Myocardial Infarction|Migraine with or Without Aura 1|Severe Covid-19|Leukemia|Leukemia, Acute Lymphoblastic|Helicobacter Pylori Infection|Hypercholesterolemia, Familial, 1|Coumarin Resistance|Pancreatic Cancer|Body Mass Index Quantitative Trait Locus 11|Respiratory Failure|Adult Respiratory Distress Syndrome|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Familial Hypercholesterolemia|Body Mass Index Quantitative Trait Locus 10
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.