Sensitive

Ischemic stroke (undetermined subtype)

ABCC1 · rs74475935

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Ischemic stroke (undetermined subtype) — no copies of the reported risk allele. (GWAS Catalog, Lancet Neurol 2015, PMID:26708676)

C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Ischemic stroke (undetermined subtype). (GWAS Catalog, Lancet Neurol 2015, PMID:26708676)

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Ischemic stroke (undetermined subtype) compared to the general population. (GWAS Catalog, Lancet Neurol 2015, PMID:26708676)

Source: GWAS Catalog, Lancet Neurol 2015, PMID:26708676

Questions about rs74475935

What is rs74475935?

rs74475935 is a single position in the genome, in or near the ABCC1 gene. Published research associates it with ischemic stroke (undetermined subtype). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs74475935 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs74475935 come from?

GWAS Catalog, Lancet Neurol 2015, PMID:26708676. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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