Variants linked to Celiac Disease

Continuously updated · newest added Oct 22, 2026

20,580 positions on this site are linked to Celiac Disease, out of 108,620 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

GPA33 protein levels

near SLC10A2 · rs9514085

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Standard

Mean corpuscular volume (UKB data field 30040)

OR5M7P · rs949359

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Standard

Platelet count (UKB data field 30080)

H2BC6-AS1 · rs9379829

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Standard

SELP protein levels

F5 · rs9332688

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Standard

FLT3LG protein levels

LINC01511 · rs9312825

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Standard

BMP4 protein levels

CAPZB · rs9287047

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Standard

CD86 protein levels

near HLA-DQB1 · rs9274932

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Standard

CD200R1 protein levels

SLC44A4 · rs9267657

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Standard

MYBPC2 protein levels

near LINC02571 · rs9265191

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Standard

Arm fat percentage right (UKB data field 23119)

near SSR3 · rs925347

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Standard

KDR protein levels

near LFNG · rs893238

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Standard

LYVE1 protein levels

PRUNE2 · rs890152

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Standard

TGFBI protein levels

near COG2 · rs853469

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Standard

Pulse rate (UKB data field 102)

near RNU6-416P · rs8048448

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Sensitive

Mean platelet thrombocyte volume (UKB data field 30100)

KALRN · rs80242847

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Standard

CCL17 protein levels

NLRC5 · rs80162955

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Standard

CRISP3 protein levels

PKHD1 · rs80047024

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Standard

Lymphocyte count (UKB data field 30120)

RASA3 · rs8001161

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Standard

High light scatter reticulocyte percentage (UKB data field 30290)

SIL1 · rs79854361

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Standard

Body fat percentage (UKB data field 23099)

LINC01569 · rs79431809

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Showing 20 of 20580 · page 7 of 1029

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.