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 118,864 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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GSTT2B protein levels

CABIN1 · rs4820582

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TNC protein levels

TNC · rs13321

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LPA protein levels

near MAP3K4-AS1 · rs1247343

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FLT4 protein levels

near RPL19P7 · rs115410474

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KRT5 protein levels

KRT5 · rs607860

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CDH5 protein levels

TSC1 · rs191754607

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ENTPD6 protein levels

HM13 · rs111303420

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Impedance of whole body (UKB data field 23106)

near ADAMTS3 · rs10518106

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FCN2 protein levels

near FCN2 · rs117532545

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IGFBP3 protein levels

IGFALS · rs35706152

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PRSS53 protein levels

near TRIM72 · rs142366936

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CLEC10A protein levels

near ASGR2 · rs62061395

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BST1 protein levels

FBXL5 · rs146796998

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F3 protein levels

SLC44A3-AS1 · rs947385

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NFASC protein levels

NFASC · rs17343527

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Mean corpuscular haemoglobin (UKB data field 30050)

TAF8 · rs9369329

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Platelet crit (UKB data field 30090)

RCL1 · rs76635833

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Glucose levels (UKB data field 30740)

SPC25 · rs71430652

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MICB or MICA protein levels

near RPL10P2 · rs11756638

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Platelet crit (UKB data field 30090)

near LINC03002 · rs9376060

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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.