Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Oct 26, 2026

1,217 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 128,364 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4

← Back to Cholesterol (LDL, HDL and Total)

Standard

HDL cholesterol x physical activity interaction (2df test)

PTTG1IP · rs235314

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Standard

HDL cholesterol x physical activity interaction (2df test)

DDB2 · rs326222

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Standard

HDL cholesterol x physical activity interaction (2df test)

DGAT2 · rs1806895

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Standard

Total cholesterol levels

DNAH11 · rs55649657

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Standard

Total cholesterol levels

near FRK · rs6932852

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Standard

Total cholesterol levels

near HLA-DQB1 · rs9275052

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Standard

Total cholesterol levels

near SDC1 · rs11899121

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Standard

Total cholesterol levels

near SDC1 · rs870527

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Low density lipoprotein cholesterol levels

APOC4-APOC2 · rs12721109

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Low density lipoprotein cholesterol levels

ZNF329 · rs34503352

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Standard

Total cholesterol levels

WHRN · rs74551598

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Low density lipoprotein cholesterol levels

TOMM40 · rs157588

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Low density lipoprotein cholesterol levels

near BCL3 · rs1531517

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Low density lipoprotein cholesterol levels

near BCL3 · rs2927439

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Low density lipoprotein cholesterol levels

ZNF235 · rs74796695

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Standard

Total cholesterol levels

ERGIC3 · rs3790136

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Standard

Total cholesterol levels

NECTIN2 · rs395908

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Standard

Total cholesterol levels

TOMM40 · rs8106922

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Standard

Low density lipoprotein cholesterol levels

near TRIB1 · rs4870941

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Standard

Low density lipoprotein cholesterol levels

NPC1L1 · rs73107473

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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.