Gene Knowledge Graph
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Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Nov 9, 2026

1,540 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,507,836 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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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

Cholesterol, total

ABCG8 · rs75331444

See detailed info → Standard

HDL cholesterol levels

MET · rs11984636

See detailed info → Standard

HDL cholesterol levels

GALNT2 · rs2144300

See detailed info → Standard

LDL cholesterol

ANXA9 · rs267733

See detailed info → Standard

LDL cholesterol

PPP1R3B · rs2169387

See detailed info → Standard

LDL cholesterol

GRINA · rs11784833

See detailed info → Standard

Cholesterol, total

CETP · rs118146573

See detailed info → Standard

LDL cholesterol

UGT1A1 · rs11563251

See detailed info → Standard

Cholesterol, total

CYP7A1 · rs2081687

See detailed info → Standard

HDL cholesterol

ANGPTL1 · rs4650994

See detailed info → Standard

LDL cholesterol

VLDLR · rs3780181

See detailed info → Standard

Cholesterol, total

HLA · rs3177928

See detailed info → Standard

Cholesterol, total

SOX17 · rs10102164

See detailed info → Standard

HDL cholesterol

ABCA1 · rs9282541

See detailed info → Standard

LDL cholesterol

IDOL · rs3757354

See detailed info → Standard

HDL cholesterol

DOCK6 · rs737337

See detailed info → Standard

HDL cholesterol

ABCA1 · rs3905000

See detailed info → Standard

Cholesterol, total

LIPG · rs149615216

See detailed info → Standard

Cholesterol, total

HP · rs11648003

See detailed info → Standard

Cholesterol, total

LPA · rs12208357

See detailed info →

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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.