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Benign nodular goiter

near OCLN · rs3846487

Where this position leads

Condition: Benign Nodular Goiter

rs3846487 Condition: Benign Nodular Goiter Benign Nodular Goiter Condition rs3846487 rs3846487 near OCLN

What the study found

Who was studied 68,987 African ancestry, admixed American, East Asian ancestry, European ancestry, South Asian ancestry, Greater Middle Eastern cases, 2,391,458 African ancestry, admixed American, East Asian ancestry, European ancestry, South Asian ancestry, Greater Middle Eastern controls.

The effect Each copy of the T allele shifted the measure 0.0552 higher (95% confidence interval 0.036-0.074); p = 1 × 10−8.

How common The T allele had a frequency of about 83% in the people studied.

Where it sits Chromosome 5, band 5q13.2 — between genes, 5.4 kb from OCLN.

What each result means

G/G Published research associates this genotype with typical/baseline likelihood of Benign nodular goiter — no copies of the reported risk allele.
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Benign nodular goiter.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Benign nodular goiter compared to the general population.
Source
Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases
White SL, Brasher MS, Pattee J, Zhou W, Chapman S, Jee YH, Bell CC, Jamil TL, Barrio M, Arehart CH, Evans LM, Hirbo J
and 73 more — show all
Cox NJ, Straub P, Namba S, Bertucci-Richter E, Guare L, Edris A, Morris S, Mulford AJ, Zhang H, Fennessy B, Tobin MD, Chen J, Williams AT, John C, van Heel DA, Mathur R, Finer S, Moksnes MR, Brumpton BM, Åsvold BO, Peculis R, Rovite V, Konrade I, Wang Y, Crooks K, Chavan S, Fisher MJ, Rafaels N, Lin M, Shortt JA, Sanders AR, Whiteman DC, MacGregor S, Medland SE, Thorsteinsdóttir U, Stefánsson K, Karaderi T, Egan KM, Bocklage T, McCrary HC, Riedlinger G, Salhia B, Shriver C, Phan MD, Farlow JL, Edge S, Kaur V, Churchman ML, Rounbehler RJ, Brock PL, Ringel MD, Pividori M, Schweppe R, Raeburn CD, Walters RG, Chen Z, Li L, Matsuda K, Okada Y, Zöllner S, Verma A, Preuss MH, Kenny E, Hendricks AE, Fishbein L, Kraft P, Daly MJ, Neale BM, Martin AR, Cole JB, Haugen BR, Gignoux CR, Pozdeyev N
Penn Medicine BioBank · Virtual Thyroid Biopsy Consortium · Colorado Center for Personalized Medicine · Genes & Health Research Team · BioBank Japan Project · Global Biobank Meta-analysis Initiative
Nature genetics · 2026 · PMID 41644669 · open access

Questions about rs3846487

What is rs3846487?

rs3846487 is a single position in the genome, in or near the near OCLN gene. Published research associates it with benign nodular goiter. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3846487 linked to?

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

Does having rs3846487 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 rs3846487 come from?

GWAS Catalog, Nature genetics 2026, PMID:41644669. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Benign nodular goiter (rs3846487). MyGeneLog™. https://www.mygenelog.com/variants/rs3846487

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