Variants linked to Celiac Disease

Continuously updated · newest added Oct 25, 2026

20,582 positions on this site are linked to Celiac Disease, out of 116,923 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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Standard

KLB protein levels

near SLC34A1 · rs4246815

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Standard

Platelet count (UKB data field 30080)

near SVIL · rs41425745

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Standard

CST7 protein levels

GGTLC1 · rs41282300

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

EEIG2 · rs41278478

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Standard

Peak expiratory flow (UKB data field 3064)

BTBD1 · rs4079029

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Standard

LRRN1 protein levels

CCDC162P · rs3941888

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Standard

SCLY protein levels

UBE2F · rs375888989

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Standard

HDL cholesterol levels (UKB data field 30760)

C4A · rs375348819

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Standard

GLIPR1 protein levels

TMEM178B · rs374826641

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Standard

GLIPR1 protein levels

SCUBE1 · rs374680689

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Standard

MSMB protein levels

near ANTXRLP1 · rs369986234

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Standard

GGT5 protein levels

near GSTT4 · rs36218313

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Standard

Peak expiratory flow (UKB data field 3064)

PKD1 · rs36103164

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Standard

NTRK3 protein levels

near NTRK3 · rs35859228

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Standard

Mean corpuscular haemoglobin (UKB data field 30050)

near SPATS2L · rs35102285

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Standard

Platelet crit (UKB data field 30090)

SCARF1 · rs34849297

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Standard

CEACAM8 protein levels

PLSCR1 · rs343316

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Standard

INHBC protein levels

LRP1 · rs34073963

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Standard

Urate levels (UKB data field 30880)

HNF4G · rs2941449

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Standard

PSAPL1 protein levels

PRSS54 · rs2897203

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Showing 20 of 20582 · page 122 of 1030

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.