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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

Low density lipoprotein cholesterol levels

near LINC01767 · rs186538116

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Low density lipoprotein cholesterol levels

LINC01755 · rs557402933

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Total cholesterol levels

near FAM117B · rs113867238

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High density lipoprotein cholesterol levels

near DYM-AS1 · rs538969346

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Total cholesterol levels

near ADAMTS3 · rs537526354

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Free cholesterol in small HDL

near HLA-DRB1 · rs111841857

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Pyruvate levels

ASH1L · rs77350683

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High density lipoprotein cholesterol levels

CD36 · rs3211938

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Total cholesterol levels

near ASGR1 · rs186021206

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Linoleic acid to total fatty acids percentage

LPL · rs286

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Average diameter for LDL particles

near LPL · rs80073370

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Cholesterol to Total Lipids in Medium LDL percentage

near LPL · rs78810414

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Free Cholesterol to Total Lipids in Medium LDL percentage

near TRIB1 · rs2954018

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Phospholipids to Total Lipids in Medium LDL percentage

near APOC1 · rs814573

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Triglycerides to Total Lipids in Small VLDL percentage

near SLC18A1 · rs7015766

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Free Cholesterol to Total Lipids in Very Small VLDL percentage

near LPL · rs1011685

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Acetoacetate levels

near SFT2D1 · rs117351628

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Triglycerides to Total Lipids in IDL percentage

near HLA-DRB1 · rs585669

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Phospholipids in large HDL

intergenic · rs9375188

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Cholesteryl Esters to Total Lipids in Large LDL percentage

near HPN · rs11671010

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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.