Sensitive

Moyamoya disease

RNF213 · rs74790219

Where this position leads

Condition: Moyamoya Disease

rs74790219 Condition: Moyamoya Disease Moyamoya Disease Condition rs74790219 rs74790219 RNF213

What the study found

Who was studied 216 Korean ancestry cases, 296 Korean ancestry controls.

The effect Each copy of the G allele carried 4.47 times the odds of Moyamoya disease (95% confidence interval 3.02-6.63); p = 9 × 10−14.

How common The G allele had a frequency of about 23% in the people studied.

Where it sits Chromosome 17, band 17q25.3 — in an intron of RNF213.

What each result means

A/A No copy of the version the research linked to Moyamoya disease. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Moyamoya disease. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Moyamoya disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs74790219

What is rs74790219?

rs74790219 is a single position in the genome, in or near the RNF213 gene. Published research associates it with moyamoya disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs74790219 linked to?

On MyGeneLog this position is linked to Moyamoya Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs74790219 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 rs74790219 come from?

GWAS Catalog, Journal of human genetics 2023, PMID:37365321. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Moyamoya disease (rs74790219). MyGeneLog™. https://www.mygenelog.com/variants/rs74790219

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