Sensitive

Autoimmune neurological syndromes with anti-GAD65 autoantibodies

LINC00879 · rs1822385

What the study found

Who was studied 167 German ancestry cases, 1,047 German ancestry controls.

The effect Each copy of the A allele carried 2.40 times the odds of Autoimmune neurological syndromes with anti-GAD65 autoantibodies (95% confidence interval 1.757-3.285); p = 4 × 10−8.

Where it sits Chromosome 3, band 3q11.2 — in an intron of LINC00879.

What each result means

A/A Two copies of the version the research linked to Autoimmune neurological syndromes with anti-GAD65 autoantibodies. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/C One copy of the version the research linked to Autoimmune neurological syndromes with anti-GAD65 autoantibodies. That is a smaller link than two copies.
C/C No copy of the version the research linked to Autoimmune neurological syndromes with anti-GAD65 autoantibodies. This is the starting point the study compared everyone against.
Source

Questions about rs1822385

What is rs1822385?

rs1822385 is a single position in the genome, in or near the LINC00879 gene. Published research associates it with autoimmune neurological syndromes with anti-gad65 autoantibodies. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1822385 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 rs1822385 come from?

GWAS Catalog, Brain : a journal of neurology 2023, PMID:35348614. 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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Autoimmune neurological syndromes with anti-GAD65 autoantibodies (rs1822385). MyGeneLog™. https://www.mygenelog.com/variants/rs1822385

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