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 2,506,432 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

TRPS1 · rs2737229

See detailed info → Standard

HDL cholesterol

SIK3 · rs11216230

See detailed info → Standard

HDL cholesterol

DAGLB · rs702485

See detailed info → Standard

Cholesterol, total

CMTM6 · rs7640978

See detailed info → Standard

Cholesterol, total

ASAP3 · rs1077514

See detailed info → Standard

HDL cholesterol

ADH5 · rs2602836

See detailed info → Standard

LDL cholesterol

LRPAP1 · rs6831256

See detailed info → Standard

LDL cholesterol

NYNRIN · rs8017377

See detailed info → Standard

LDL cholesterol

PIGV · rs12748152

See detailed info → Standard

LDL cholesterol

LOC84931 · rs2030746

See detailed info → Standard

LDL cholesterol

MTMR3 · rs5763662

See detailed info → Standard

LDL cholesterol

INSIG2 · rs10490626

See detailed info → Standard

HDL cholesterol

CD36 · rs2366858

See detailed info → Standard

Cholesterol, total

UBASH3B · rs7941030

See detailed info → Standard

Cholesterol, total

RAF1 · rs2290159

See detailed info → Standard

Cholesterol, total

PHLDB1 · rs11603023

See detailed info → Standard

Cholesterol, total

PPARA · rs4253772

See detailed info → Standard

Cholesterol, total

PLEC1 · rs11136341

See detailed info → Standard

Cholesterol, total

PXK · rs13315871

See detailed info → Standard

Response to fenofibrate

AHCYL2 · rs11766298

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.