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 113,783 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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VNN2 protein levels

ANKRD44 · rs11888210

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Platelet count (UKB data field 30080)

CUX2 · rs118185626

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GLIPR1 protein levels

VAV2 · rs118109295

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LRP11 protein levels

PPP1R14C · rs11752228

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SUSD2 protein levels

N4BP1 · rs11641641

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TOR1AIP1 protein levels

near CEP350 · rs115939179

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CDCP1 protein levels

CDCP1 · rs114658092

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TOR1AIP1 protein levels

near LINC02818 · rs113876953

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OPTC protein levels

near RSPO1 · rs11264079

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BTC protein levels

near AREG · rs112568214

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DHRS4L2 protein levels

TGM1 · rs112204670

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KLB protein levels

ABCA5 · rs111923967

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Mean corpuscular haemoglobin (UKB data field 30050)

NFIX · rs111875145

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MEPE protein levels

RPS6KA5 · rs11159982

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CD302 protein levels

BAZ2B · rs10489999

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CD1C protein levels

SEC23A · rs10141243

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CD160 protein levels

near IL15 · rs10008383

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ALCAM protein levels

DOK7 · rs10007119

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Red blood cell erythrocyte count (UKB data field 30010)

LNCTSI · rs9977315

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Mean sphered cell volume (UKB data field 30270)

YWHAE · rs9915564

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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.