Sensitive

Obstetric antiphospholipid syndrome

C1D · rs79154414

Where this position leads

Condition: Obstetric Antiphospholipid Syndrome

rs79154414 Condition: Obstetric Antiphospholipid Syndrome Obstetric Antiphospholipid Syndrome Condition rs79154414 rs79154414 C1D

What the study found

Who was studied 115 Japanese ancestry female cases, 419 Japanese ancestry male and female controls.

The effect Each copy of the T allele carried 6.20 times the odds of Obstetric antiphospholipid syndrome (95% confidence interval 2.96-13.0); p = 5 × 10−8.

How common The T allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 2, band 2p14 — between genes, 71.4 kb from LINC01812.

What each result means

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

Questions about rs79154414

What is rs79154414?

rs79154414 is a single position in the genome, in or near the C1D gene. Published research associates it with obstetric antiphospholipid syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs79154414 linked to?

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

Does having rs79154414 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 rs79154414 come from?

GWAS Catalog, J Hum Genet 2017, PMID:28424481. 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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Obstetric antiphospholipid syndrome (rs79154414). MyGeneLog™. https://www.mygenelog.com/variants/rs79154414

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