Gene Knowledge Graph
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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.

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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

DOCK7 · rs10889333

See detailed info → Standard

Cholesterol, total

APOE · rs7412

See detailed info → Standard

Response to statins (HDL cholesterol change)

CETP · rs247616

See detailed info → Standard

HDL cholesterol

ABCA1 · rs2575876

See detailed info → Standard

LDL cholesterol

MAFB · rs1883711

See detailed info → Standard

LDL cholesterol

CILP2 · rs73001065

See detailed info → Standard

LDL cholesterol

LPA · rs186696265

See detailed info → Standard

LDL cholesterol

NYNRIN · rs11621792

See detailed info → Standard

HDL cholesterol

HDGF · rs12145743

See detailed info → Standard

HDL cholesterol

CETP · rs247617

See detailed info → Standard

Cholesterol, total

A2ML1 · rs4883201

See detailed info → Standard

HDL cholesterol

NLRC5 · rs1532624

See detailed info → Standard

HDL cholesterol

LIPC · rs1077835

See detailed info → Standard

LDL cholesterol

HPR · rs2000999

See detailed info → Standard

HDL cholesterol

LCAT · rs16942887

See detailed info → Standard

Cholesterol, total

APOB · rs693

See detailed info → Standard

Cholesterol, total

LDLR · rs112374545

See detailed info → Standard

Cholesterol, total

LIPC · rs1601935

See detailed info → Standard

Cholesterol, total

APOB · rs1041968

See detailed info → Standard

HDL cholesterol

LIPC · rs10468017

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.