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SKAP1 · rs16955463
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.
Strength of the evidence
Its strongest genetic-study result is p = 10−9, with 1 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 6,952 European ancestry cases, 42,436 European ancestry controls, 118 African ancestry cases, 3,680 African ancestry controls, 337 Asian ancestry cases, 6,422 Asian ancestry controls.
The effect The reported allele is T; the catalogue records no effect size ; p = 2 × 10−9.
Where it sits Chromosome 17, band 17q21.32 — in an intron of SKAP1.
How common each version is
GT
G 86.2% · T 13.8%
G 87.2% · T 12.8%
G 85.8% · T 14.2%
G 90.0% · T 10.0%
G 92.6% · T 7.4%
G 80.2% · T 19.8%
G 82.0% · T 18.0%
G 82.3% · T 17.7%
The share of all copies of this position that are each version. Source: the population studies published in dbSNP (US NCBI); each row names its study.
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Genetic generalized epilepsy (rs16955463). MyGeneLog™. https://www.mygenelog.com/variants/rs16955463