Variants linked to Celiac Disease

Continuously updated · newest added Oct 26, 2026

20,582 positions on this site are linked to Celiac Disease, out of 128,364 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4

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Standard

GPR37 protein levels

near RNU6-102P · rs748476794

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Standard

TBC1D17 protein levels

FUZ · rs74590950

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Standard

FOLR3 protein levels

SHANK2 · rs73521130

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Standard

Alkaline phosphatase (UKB data field 30610)

near OASL2P · rs73419642

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Standard

CD83 protein levels

BTNL2 · rs73400847

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Standard

OLFM4 protein levels

near PCDH8 · rs73192409

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

PIK3CG · rs73186297

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Standard

IL17D protein levels

EEF1AKMT1 · rs73167412

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Standard

Creatinine levels (UKB data field 30700)

PSMD6-AS2 · rs73119034

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Standard

CLSTN3 protein levels

near ACSM4 · rs73057723

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Standard

Alkaline phosphatase (UKB data field 30610)

LINC02714 · rs73030001

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Standard

TREH protein levels

near TMPRSS13 · rs73024419

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Standard

MASP1 protein levels

near CWC22 · rs72958838

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Standard

CFP protein levels

near MTCO1P54 · rs72926960

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Standard

VEGFA protein levels

near LINC02537 · rs72863914

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Standard

UMOD protein levels

PROM2 · rs72819488

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Standard

RET protein levels

near RET · rs72781205

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Standard

HLA A protein levels

B3GALT4 · rs72654500

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Standard

ENPP7 protein levels

near LINC01979 · rs71387950

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Standard

Triglyceride levels (UKB data field 30870)

near RPL37AP8 · rs7114594

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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.