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

Free Cholesterol to Total Lipids in Large LDL percentage

PSKH1 · rs56070533

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Triglycerides to Total Lipids in Large LDL percentage

intergenic · rs465002

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Cholesterol to Total Lipids in Large VLDL percentage

JAZF1 · rs849138

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Cholesteryl Esters to Total Lipids in Large VLDL percentage

GALNT2 · rs10779835

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Cholesteryl Esters to Total Lipids in Large VLDL percentage

near KLF14 · rs11762784

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Triglycerides to Total Lipids in Large VLDL percentage

HNF1A · rs9738226

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Linoleic acid to total fatty acids percentage

near MOGAT2 · rs531117

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Triglycerides in LDL

TRPS1 · rs2737263

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Cholesteryl Esters to Total Lipids in Medium HDL percentage

near BMP8A · rs72663520

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Cholesteryl Esters in Medium HDL

AKNA · rs10733608

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Concentration of medium HDL particles

APOC3 · rs12721030

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Phospholipids to Total Lipids in Medium HDL percentage

near USP1 · rs626787

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Triglycerides to Total Lipids in Medium VLDL percentage

ABCA9 · rs78196338

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Omega-6 fatty acids to total fatty acids percentage

DOCK7 · rs10889334

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Phosphoglycerides levels

near MICB · rs3094012

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Polyunsaturated fatty acids to total fatty acids percentage

RIC8B · rs3782709

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Free Cholesterol to Total Lipids in Small LDL percentage

near TMEM263 · rs10861678

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Phospholipids to Total Lipids in Small LDL percentage

near MOGAT2 · rs559355

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Free cholesterol in small VLDL

CATSPER2 · rs141866277

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Free cholesterol in small VLDL

MLXIPL · rs77048596

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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.