Variants linked to Celiac Disease

Continuously updated · newest added Oct 23, 2026

20,580 positions on this site are linked to Celiac Disease, out of 109,838 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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C1QTNF9 protein levels

SPATA13 · rs147864790

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High light scatter reticulocyte percentage (UKB data field 30290)

DOCK3 · rs147794010

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VSNL1 protein levels

near PSMC1P10 · rs147698583

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GLIPR1 protein levels

VOPP1 · rs147692885

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ENPP7 protein levels

TBC1D16 · rs147673750

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SETMAR protein levels

SUMF1 · rs147614904

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PCDH9 protein levels

PCDH9 · rs147587099

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TFF3 protein levels

HLA-B · rs147412087

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FNDC1 protein levels

near LINC02529 · rs147377860

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VNN1 protein levels

near VNN3P · rs147172620

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LPL protein levels

HTRA1-AS1 · rs147005763

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OLFM4 protein levels

NEK3 · rs146936497

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GSTT2B protein levels

DDTL · rs146700008

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FAS protein levels

FAS · rs146676863

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GLIPR1 protein levels

PPP4R4 · rs146647817

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TNR protein levels

LINC01820 · rs146610421

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Gamma glutamyltransferase levels (UKB data field 30730)

AMN · rs146499374

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FCER2 protein levels

SREBF2 · rs146427423

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FLRT2 protein levels

FLRT2 · rs146363556

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MST1 protein levels

ZNF589 · rs146138122

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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.