Standard
Thyroid hormone levels
LHX3 · rs7860634
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 each result means
A/A
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Thyroid hormone levels compared to the general population. (GWAS Catalog, PLoS Genet 2013, PMID:23408906)
A/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Thyroid hormone levels. (GWAS Catalog, PLoS Genet 2013, PMID:23408906)
G/G
Published research associates this genotype with typical/baseline likelihood of Thyroid hormone levels — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2013, PMID:23408906)
Source
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function
Porcu E,
Medici M,
Pistis G,
Volpato CB,
Wilson SG,
Cappola AR,
Bos SD,
Deelen J,
den Heijer M,
Freathy RM,
Lahti J,
Liu C
and 82 more — show all
Lopez LM,
Nolte IM,
O'Connell JR,
Tanaka T,
Trompet S,
Arnold A,
Bandinelli S,
Beekman M,
Böhringer S,
Brown SJ,
Buckley BM,
Camaschella C,
de Craen AJ,
Davies G,
de Visser MC,
Ford I,
Forsen T,
Frayling TM,
Fugazzola L,
Gögele M,
Hattersley AT,
Hermus AR,
Hofman A,
Houwing-Duistermaat JJ,
Jensen RA,
Kajantie E,
Kloppenburg M,
Lim EM,
Masciullo C,
Mariotti S,
Minelli C,
Mitchell BD,
Nagaraja R,
Netea-Maier RT,
Palotie A,
Persani L,
Piras MG,
Psaty BM,
Räikkönen K,
Richards JB,
Rivadeneira F,
Sala C,
Sabra MM,
Sattar N,
Shields BM,
Soranzo N,
Starr JM,
Stott DJ,
Sweep FC,
Usala G,
van der Klauw MM,
van Heemst D,
van Mullem A,
Vermeulen SH,
Visser WE,
Walsh JP,
Westendorp RG,
Widen E,
Zhai G,
Cucca F,
Deary IJ,
Eriksson JG,
Ferrucci L,
Fox CS,
Jukema JW,
Kiemeney LA,
Pramstaller PP,
Schlessinger D,
Shuldiner AR,
Slagboom EP,
Uitterlinden AG,
Vaidya B,
Visser TJ,
Wolffenbuttel BH,
Meulenbelt I,
Rotter JI,
Spector TD,
Hicks AA,
Toniolo D,
Sanna S,
Peeters RP,
Naitza S
PLoS genetics · 2013 · PMID 23408906 · open access
Questions about rs7860634
What is rs7860634?
rs7860634 is a single position in the genome, in or near the LHX3 gene. Published research associates it with thyroid hormone levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs7860634 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 rs7860634 come from?
GWAS Catalog, PLoS Genet 2013, PMID:23408906. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants