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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Recommended (connected, strongest) Strongest evidence Newest Oldest

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

Total cholesterol levels

SMARCA4 · rs17001095

See detailed info → Standard

Total cholesterol levels

SMARCA4 · rs3786722

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High density lipoprotein cholesterol levels

MAPK8IP1 · rs77403571

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Low density lipoprotein cholesterol levels

POC5 · rs34361

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Low density lipoprotein cholesterol levels

ABCG8 · rs4953023

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Low density lipoprotein cholesterol levels

SPRY3 · rs306890

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Low density lipoprotein cholesterol levels

USP24 · rs191448950

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Low density lipoprotein cholesterol levels

USP24 · rs287227

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Total cholesterol levels

ST3GAL4 · rs10893499

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High density lipoprotein cholesterol levels

near PLTP · rs4810479

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High density lipoprotein cholesterol levels

PEPD · rs4805881

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High density lipoprotein cholesterol levels

near MPP3 · rs149580368

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High density lipoprotein cholesterol levels

NUTF2 · rs1124324

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High density lipoprotein cholesterol levels

RANBP10 · rs73591976

See detailed info → Standard

High density lipoprotein cholesterol levels

SLC12A4 · rs3785100

See detailed info → Standard

High density lipoprotein cholesterol levels

CETP · rs9923854

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High density lipoprotein cholesterol levels

CETP · rs2303790

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High density lipoprotein cholesterol levels

near CETP · rs17231520

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High density lipoprotein cholesterol levels

FRMD5 · rs138570705

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High density lipoprotein cholesterol levels

TTBK2 · rs149492745

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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.