ADGRB3 · rs117763955
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 = 10−7, 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 991 Korean ancestry middle-aged cases, 21,921 Korean ancestry middle-aged controls.
The effect The reported allele is T; the catalogue records no effect size ; p = 4 × 10−8.
How common The T allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 6, band 6q13 — in an intron of ADGRB3.
rs117763955 is a single position in the genome, in or near the ADGRB3 gene. Published research associates it with underweight. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
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.
GWAS Catalog, Journal of human nutrition and dietetics : the official journal of the British Dietetic Association 2023, PMID:36632775. 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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Underweight (rs117763955). MyGeneLog™. https://www.mygenelog.com/variants/rs117763955