Variants linked to Diverticular Disease

Continuously updated · newest added Oct 7, 2026

32 positions on this site are linked to Diverticular Disease, out of 51,109 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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Sensitive

Diverticular disease

NALF1 · rs16970678

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Sensitive

Diverticular disease

ARHGAP15-AS1 · rs71350022

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Sensitive

Diverticular disease

ARHGAP15 · rs10179961

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Sensitive

Diverticular disease

TWF2 · rs352143

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Sensitive

Diverticular disease

ANO1 · rs2276068

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Standard

Diverticulosis and diverticulitis (PheCode 562)

BMPR1B · rs7673527

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Standard

Diverticulosis and diverticulitis (PheCode 562)

ARHGAP15 · rs4372823

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Standard

Diverticulosis (PheCode 562.1)

FBXL13 · rs7800548

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Sensitive

Diverticular disease

near COL6A1 · rs9983489

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Sensitive

Diverticular disease

NALF1 · rs9514637

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Standard

Diverticulosis (PheCode 562.1)

CALCB · rs2132469

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Standard

Diverticulosis and diverticulitis (PheCode 562)

CALCB · rs12294208

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Sensitive

Diverticular disease

TNS1 · rs1427669

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Standard

Diverticulosis and diverticulitis (PheCode 562)

near COL6A1 · rs8131409

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Sensitive

Diverticular disease

near EFEMP1 · rs11899380

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Sensitive

Diverticular disease

ENSG00000251283 · rs11934833

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Sensitive

Diverticular disease

ELN · rs3823878

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Sensitive

Diverticular disease

RBKS · rs10173528

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Sensitive

Diverticular disease

NOV · rs1381335

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Sensitive

Diverticular disease

UNC50 · rs148376933

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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.