Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Oct 25, 2026

1,155 positions on this site are linked to Cholesterol (LDL, HDL and Total), 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.

← Back to Cholesterol (LDL, HDL and Total)

Standard

LDL cholesterol x physical activity interaction (2df test)

near CYP7A1 · rs9297994

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LDL cholesterol x physical activity interaction (2df test)

near SMARCA4 · rs114846969

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LDL cholesterol x physical activity interaction (2df test)

near TMED4 · rs217358

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LDL cholesterol x physical activity interaction (2df test)

ABCA6 · rs117753190

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LDL cholesterol x physical activity interaction (2df test)

MAMSTR · rs4002471

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LDL cholesterol x physical activity interaction (2df test)

MACO1 · rs12027110

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LDL cholesterol x physical activity interaction (2df test)

near HNF1A · rs6489786

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LDL cholesterol x physical activity interaction (2df test)

near IRF2BP2 · rs556107

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Low density lipoprotein cholesterol levels

HAVCR1 · rs17573010

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High density lipoprotein cholesterol levels

NLRC5 · rs1875236

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High density lipoprotein cholesterol levels

near CETP · rs17369163

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LDL cholesterol x physical activity interaction (2df test)

near DDX18 · rs72834327

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Standard

LDL cholesterol x physical activity interaction (2df test)

near C2CD2 · rs116376114

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Total cholesterol levels

LRRK2 · rs1907631

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Total cholesterol levels

CCDC170 · rs9371220

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LDL cholesterol levels

ACAD11 · rs17345563

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LDL cholesterol levels

ST3GAL4 · rs17135399

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LDL cholesterol levels

ANGPTL3 · rs11485618

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LDL cholesterol levels

CYP7A1 · rs13277801

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LDL cholesterol levels

IRF2BP2 · rs2587534

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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.