Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,581 positions on this site are linked to Celiac Disease, out of 111,015 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Standard

Triglyceride levels (UKB data field 30870)

C5orf67 · rs34196215

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Standard

DCDC2C protein levels

near HLA-DQB1 · rs28891435

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Standard

TMPRSS11D protein levels

near GPR166P · rs236448

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Direct low density lipoprotein levels (UKB data field 30780)

CKM · rs1967311

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Standard

CFHR2 protein levels

DENND1B · rs193149367

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Standard

ENPP2 protein levels

TAF2 · rs191996426

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C1QTNF9 protein levels

RNF17 · rs191501886

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TNC protein levels

TNC · rs191399342

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OGN protein levels

near BEND3P2 · rs191144742

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CTSC protein levels

near Y_RNA · rs190603325

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IL17RB protein levels

near SELENOK · rs189712140

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SUSD5 protein levels

near CCR4 · rs187957635

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RNF149 protein levels

near PRCPP1 · rs186294975

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GLIPR1 protein levels

FLI1 · rs185115437

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IL17RA protein levels

near IL17RA · rs185109070

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Standard

IL17RA protein levels

GAB4 · rs182948629

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

RTTN · rs182906071

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Standard

GLIPR1 protein levels

SPECC1 · rs181489620

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Standard

IFNGR2 protein levels

IFNGR2 · rs17885472

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Impedance of whole body (UKB data field 23106)

LINC01847 · rs17057165

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Showing 20 of 20581 · page 38 of 1030

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.