Variants linked to Hypothyroidism

Continuously updated · newest added Sep 30, 2026

249 positions on this site are linked to Hypothyroidism, out of 22,484 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

SIK3 · rs4938330

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Hypothyroidism

near ETS1 · rs73018928

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Hypothyroidism

FLI1 · rs7113735

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Hypothyroidism

B4GALNT3 · rs150722154

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Hypothyroidism

NINJ2 · rs60759266

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Hypothyroidism

near CD69 · rs199546043

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Hypothyroidism

near ETV6 · rs2954930

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Hypothyroidism

near SCAF11 · rs4768675

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Hypothyroidism

RAPGEF3 · rs11830537

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Hypothyroidism

OR6C74 · rs187123775

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Hypothyroidism

near RPS26 · rs61938963

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Hypothyroidism

near PTGES3 · rs11171914

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Hypothyroidism

C12orf42 · rs12582330

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Hypothyroidism

SPATA13 · rs7327973

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Hypothyroidism

near PDS5B · rs12323101

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Hypothyroidism

near MAF · rs73575083

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Hypothyroidism

MIEN1 · rs4252665

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Hypothyroidism

LRRC37A2 · rs11651642

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Hypothyroidism

SEC14L1 · rs2053568

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Hypothyroidism

near TMEM235 · rs12952267

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Showing 20 of 249 · page 5 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.