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Free thyroxine concentration

SOX2_OT · rs6785807

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.

What the study found

Who was studied 49,269 European ancestry individuals; replicated in up to 22,383 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.057 lower (95% confidence interval 0.039-0.075); p = 7 × 10⁻¹¹.

How common The A allele had a frequency of about 15% in the people studied.

Where it sits Chromosome 3, band 3q26.33 — in an intron of LINC01206.

What each result means

A/A Two copies of the version the research linked to Free thyroxine concentration. That is the strongest link of the three results. A link in a study is not a diagnosis.

A/G One copy of the version the research linked to Free thyroxine concentration. That is a smaller link than two copies.

G/G No copy of the version the research linked to Free thyroxine concentration. This is the starting point the study compared everyone against.

Source

Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation

Teumer A, Chaker L, Groeneweg S, Li Y, Di Munno C, Barbieri C, Schultheiss UT, Traglia M, Ahluwalia TS, Akiyama M, Appel EVR, Arking DE

and 116 more — show all

Arnold A, Astrup A, Beekman M, Beilby JP, Bekaert S, Boerwinkle E, Brown SJ, De Buyzere M, Campbell PJ, Ceresini G, Cerqueira C, Cucca F, Deary IJ, Deelen J, Eckardt KU, Ekici AB, Eriksson JG, Ferrrucci L, Fiers T, Fiorillo E, Ford I, Fox CS, Fuchsberger C, Galesloot TE, Gieger C, Gögele M, De Grandi A, Grarup N, Greiser KH, Haljas K, Hansen T, Harris SE, van Heemst D, den Heijer M, Hicks AA, den Hollander W, Homuth G, Hui J, Ikram MA, Ittermann T, Jensen RA, Jing J, Jukema JW, Kajantie E, Kamatani Y, Kasbohm E, Kaufman JM, Kiemeney LA, Kloppenburg M, Kronenberg F, Kubo M, Lahti J, Lapauw B, Li S, Liewald DCM, Lim EM, Linneberg A, Marina M, Mascalzoni D, Matsuda K, Medenwald D, Meisinger C, Meulenbelt I, De Meyer T, Meyer Zu Schwabedissen HE, Mikolajczyk R, Moed M, Netea-Maier RT, Nolte IM, Okada Y, Pala M, Pattaro C, Pedersen O, Petersmann A, Porcu E, Postmus I, Pramstaller PP, Psaty BM, Ramos YFM, Rawal R, Redmond P, Richards JB, Rietzschel ER, Rivadeneira F, Roef G, Rotter JI, Sala CF, Schlessinger D, Selvin E, Slagboom PE, Soranzo N, Sørensen TIA, Spector TD, Starr JM, Stott DJ, Taes Y, Taliun D, Tanaka T, Thuesen B, Tiller D, Toniolo D, Uitterlinden AG, Visser WE, Walsh JP, Wilson SG, Wolffenbuttel BHR, Yang Q, Zheng HF, Cappola A, Peeters RP, Naitza S, Völzke H, Sanna S, Köttgen A, Visser TJ, Medici M

Lifelines Cohort Study

Nature communications · 2018 · PMID 30367059 · open access

Questions about rs6785807

What is rs6785807?

rs6785807 is a single position in the genome, in or near the SOX2_OT gene. Published research associates it with free thyroxine concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6785807 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 rs6785807 come from?

GWAS Catalog, Nature communications 2018, PMID:30367059. 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.

Free thyroxine concentration (rs6785807). MyGeneLog™. https://www.mygenelog.com/variants/rs6785807

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