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 115,968 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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RIDA protein levels

near POP1 · rs141954885

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SNCG protein levels

GLUD1 · rs141631853

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THTPA protein levels

NGDN · rs141291730

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VWF protein levels

GBGT1 · rs141083020

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OSMR protein levels

RICTOR · rs140903617

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DDR1 protein levels

near RN7SKP186 · rs140832937

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Creatinine levels (UKB data field 30700)

SLC30A4 · rs140824560

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Immature reticulocyte fraction (UKB data field 30280)

near TRIM58 · rs140799900

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IL6R protein levels

TDRD10 · rs140443118

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ENDOU protein levels

RPAP3 · rs140206815

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CRISP3 protein levels

near CRISP1 · rs139691348

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GSTM4 protein levels

GNAT2 · rs139606823

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REG3G protein levels

near REG3G · rs139475952

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TNN protein levels

RABGAP1L · rs139464224

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TSPAN8 protein levels

TSPAN8 · rs139203205

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KIR3DL1 protein levels

NCR1 · rs139123108

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KLK1 protein levels

SEC1P · rs138919976

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DKK3 protein levels

STAB2 · rs138758541

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FUCA1 protein levels

ELOA-AS1 · rs138727921

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CD160 protein levels

near CD160 · rs138614809

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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.