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Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Nov 8, 2026

1,538 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,506,722 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 Connections: all only those linked to a condition, drug or sense

← Back to Cholesterol (LDL, HDL and Total)

Standard

High density lipoprotein cholesterol levels

near MOGAT2 · rs600518

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Standard

High density lipoprotein cholesterol levels

ABCA1 · rs2740488

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Standard

High density lipoprotein cholesterol levels

near LPL · rs17489282

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Standard

High density lipoprotein cholesterol levels

near SLC18A1 · rs6999158

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Standard

High density lipoprotein cholesterol levels

near LPL · rs79236614

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Standard

High density lipoprotein cholesterol levels

near LPL · rs28526159

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Standard

High density lipoprotein cholesterol levels

MLXIPL · rs13240994

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Standard

High density lipoprotein cholesterol levels

near PRKAG3 · rs78058190

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High density lipoprotein cholesterol levels

near COBLL1 · rs10184004

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Standard

High density lipoprotein cholesterol levels

APOB · rs533617

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Standard

High density lipoprotein cholesterol levels

near APOB · rs13392272

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Standard

LDL cholesterol x physical activity interaction (2df test)

near SMARCA4 · rs114846969

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Standard

LDL cholesterol x physical activity interaction (2df test)

near CYP7A1 · rs9297994

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Standard

LDL cholesterol x physical activity interaction (2df test)

near TOP1 · rs6029549

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Standard

High density lipoprotein cholesterol levels

NLRC5 · rs1875236

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LDL cholesterol levels

ANGPTL3 · rs11485618

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HDL cholesterol levels

LPL · rs7841189

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Total cholesterol levels

LIPG · rs9958734

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Total cholesterol levels

ANGPTL3 · rs11208004

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Cholesterol, total

CERT1 · rs6873472

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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.