Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 117,690 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

TNC protein levels

LINC01091 · rs17007241

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Standard

PAEP protein levels

NACC2 · rs151219465

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Standard

GBP4 protein levels

GBP2 · rs151076206

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Standard

CSTB protein levels

near LINC00313 · rs150534755

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Standard

ATXN3 protein levels

TRIP11 · rs149907296

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Standard

RARRES1 protein levels

RSRC1 · rs148810927

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Standard

DCBLD2 protein levels

near RPL19P7 · rs148301528

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Standard

INHBB protein levels

near LINC01101 · rs146999772

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

NSRP1 · rs146976827

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Standard

DRAXIN protein levels

near LINC01647 · rs145145201

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Standard

EDAR protein levels

EDAR · rs144796586

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Creatinine levels (UKB data field 30700)

CCDC26 · rs1441993

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VSTM1 protein levels

near CACNG6 · rs143962230

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Standard

CAPG protein levels

DNAH6 · rs138838654

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Standard

MME protein levels

NEK4 · rs138522038

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Standard

Pulse rate (UKB data field 102)

TTN · rs13021201

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Standard

AMN protein levels

near RAP2CP1 · rs12891232

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Total protein levels (UKB data field 30860)

FGFR1 · rs12677006

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Standard

IGF 1 (UKB data field 30770)

PLEC · rs12549853

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Standard

Peak expiratory flow (UKB data field 3064)

FIG4 · rs12203993

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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.