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Lymphocytic thyroiditis

TG · rs114322847

Where this position leads

Condition: Lymphocytic Thyroiditis (Hashimoto's)

rs114322847 Condition: Lymphocytic Thyroiditis (Hashimoto's) Lymphocytic Thyroiditis (Hashimoto's) Condition rs114322847 rs114322847 TG

What the study found

Who was studied 15,106 European ancestry cases, 1,405,552 European ancestry controls.

The effect Each copy of the T allele shifted the measure 0.372 higher (95% confidence interval 0.29-0.45); p = 1 × 10−18.

How common The T allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 8, band 8q24.22 — a missense change in TG.

What ClinVar records

Classification Conflicting classifications of pathogenicity for Iodotyrosyl coupling defect; criteria provided, conflicting classifications (1 of 4 stars, 6 submitters), last evaluated 2026-06-01. ClinVar record 910761 NM_003235.5(TG):c.353C>T (p.Pro118Leu)

What this is ClinVar's aggregate record for this position (as of its 2026-09-24 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Lymphocytic thyroiditis — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Lymphocytic thyroiditis.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Lymphocytic thyroiditis compared to the general population.
Source

Questions about rs114322847

What is rs114322847?

rs114322847 is a single position in the genome, in or near the TG gene. Published research associates it with lymphocytic thyroiditis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs114322847 linked to?

On MyGeneLog this position is linked to Lymphocytic Thyroiditis (Hashimoto's). The research behind each link, and its sources, are set out on that condition page.

Does having rs114322847 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 rs114322847 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.

Lymphocytic thyroiditis (rs114322847). MyGeneLog™. https://www.mygenelog.com/variants/rs114322847

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