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 110,175 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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TIMP3 protein levels

BET1L · rs143674792

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IGFBP3 protein levels

SSTR5 · rs4988483

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FUT3 or FUT5 protein levels

near SLCO1B1 · rs58989256

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IGF2R protein levels

near VN1R10P · rs56401801

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OXT protein levels

TUBGCP4 · rs149181595

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BPIFA2 protein levels

MAMSTR · rs117062744

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RET protein levels

NPAS2 · rs6747755

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GUSB protein levels

ELF1 · rs17532371

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MFGE8 protein levels

near HLA-DRB1 · rs11751673

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Trunk fat mass (UKB data field 23128)

near SYT4 · rs2052607

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Standing height (UKB data field 50)

COL14A1 · rs56311349

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PXN protein levels

near HLA-DQB1 · rs28414666

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PRSS27 protein levels

SULT2B1 · rs117085958

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TPP1 protein levels

TMEM131L · rs78947501

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MOCS2 protein levels

near NRF1 · rs6967348

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CST1 protein levels

near AMY1C · rs72694438

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PLA2G1B protein levels

near RSPO3 · rs4318902

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MFGE8 protein levels

near LINC02702 · rs144788484

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TCL1A protein levels

SPMIP7 · rs116968179

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IGF1R protein levels

near ABO · rs72775457

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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.