Variants linked to Celiac Disease

Continuously updated · newest added Oct 24, 2026

20,582 positions on this site are linked to Celiac Disease, out of 113,994 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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THBS2 protein levels

MICA-AS1 · rs1052409

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ACP5 protein levels

CPN1 · rs4919420

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Alkaline phosphatase (UKB data field 30610)

near GPX4 · rs2075710

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TNR protein levels

SLC38A4-AS1 · rs4768704

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Creatinine levels (UKB data field 30700)

SBF1 · rs1053764

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CNTN2 protein levels

RREB1 · rs4959426

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FRZB protein levels

near RNU6ATAC · rs4994332

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HMOX1 protein levels

HABP2 · rs41292628

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ARG1 protein levels

NFIX · rs34720245

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UBE2L6 protein levels

near RPS4XP13 · rs2729356

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MEPE protein levels

IL11RA · rs11575580

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High light scatter reticulocyte percentage (UKB data field 30290)

near MPP2 · rs1072235

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Weight (UKB data field 21002)

TMEM244 · rs9321191

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TFRC protein levels

near H1-4 · rs9358909

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STAB2 protein levels

STKLD1 · rs113845480

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GNAS protein levels

HCG22 · rs9262651

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PAIP2B protein levels

near HLA-DQB1 · rs13208948

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LGALS3 protein levels

CD163L1 · rs765911263

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CA3 protein levels

near LINC00184 · rs72749982

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MDK protein levels

near HCG27 · rs6927324

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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.