Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Oct 26, 2026

422 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 134,364 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

← Back to Cholesterol (LDL, HDL and Total)

Standard

Glucose levels

near BTBD7P2 · rs10885120

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HDL cholesterol

ACP2 · rs75393320

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Phospholipids to Total Lipids in Large HDL percentage

SLC22A3 · rs673736

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Free cholesterol in small HDL

near HLA-DRB1 · rs111841857

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Cholesteryl Esters in Small HDL

near TPM1 · rs2134263

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LDL cholesterol

HMGCR · rs12654264

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Phospholipids to Total Lipids in Small HDL percentage

near ASGR1 · rs72837682

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LDL cholesterol

LINC01830 · rs145030841

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Pyruvate levels

ASH1L · rs77350683

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Cholesterol in Small HDL

near RPL5P6 · rs662026

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Glutamine levels

CATSPER2 · rs139097404

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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 in small HDL

TMPRSS11E · rs4694077

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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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Free Cholesterol to Total Lipids in Chylomicrons and Extremely Large VLDL percentage

near SLC18A1 · rs4128744

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Showing 20 of 422 · page 2 of 22

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.