Variants linked to Hypothyroidism

Continuously updated · newest added Sep 30, 2026

249 positions on this site are linked to Hypothyroidism, out of 22,358 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Hypothyroidism

Standard

Hypothyroidism

CAPZB · rs75491569

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Standard

Free thyroxine concentration

ID4 · rs10946313

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Standard

Free thyroxine concentration

NCOR1 · rs11078333

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Standard

Hypothyroidism

FMNL1 · rs12449792

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Standard

Free thyroxine concentration

DIO2 · rs225014

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Standard

Free thyroxine concentration

CA8 · rs67583169

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Standard

Hypothyroidism

PDE10A · rs2983514

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Standard

Hypothyroidism

TPO · rs11675342

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Standard

Hypothyroidism

HLA-C · rs2517532

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Showing 9 of 249 · page 13 of 13

Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.