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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

LDL cholesterol

near APOB · rs577584

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Standard

HDL cholesterol

TRPS1 · rs12543799

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HDL cholesterol

near LILRA5 · rs380267

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HDL cholesterol

near LPL · rs79407615

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Low density lipoprotein cholesterol levels

near TDRD15 · rs1712248

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High density lipoprotein cholesterol levels

NR1H3 · rs10838684

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Total cholesterol levels

ST3GAL4 · rs74612335

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Total cholesterol levels

near RASSF6 · rs573930512

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Total cholesterol levels

HP · rs5471

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Total cholesterol levels

FUT2 · rs516246

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High density lipoprotein cholesterol levels

near BUD13 · rs138449252

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Triglycerides in very small VLDL

JMJD1C · rs7909269

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High density lipoprotein cholesterol levels

near LINC02702 · rs541102880

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Low density lipoprotein cholesterol levels

KPNB1-DT · rs12603290

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LDL cholesterol

PCSK9 · rs564427867

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Total cholesterol levels

APOB · rs57825321

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Concentration of HDL particles

APOC3 · rs4225

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Low density lipoprotein cholesterol levels

USP1 · rs598253

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Total cholesterol levels

DOCK7 · rs11207980

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Citrate levels

ANKH · rs10065666

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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.