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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 2,506,771 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

EHBP1 · rs4671050

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Total cholesterol levels

near LINC01822 · rs147821144

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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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Cholesteryl Esters in Small HDL

near TPM1 · rs2134263

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Low density lipoprotein cholesterol levels

near RNU2-62P · rs35657082

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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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Low density lipoprotein cholesterol levels

B4GALNT3 · rs35882350

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LDL cholesterol

LINC01830 · rs145030841

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Total cholesterol levels

PGS1 · rs11657987

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Total cholesterol levels

ABCB11 · rs10184673

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Cholesterol in Small HDL

near RPL5P6 · rs662026

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Glutamine levels

CATSPER2 · rs139097404

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Triglycerides in small HDL

TMPRSS11E · rs4694077

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

near SLC18A1 · rs4128744

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Triglycerides in large HDL

near C12orf42 · rs7298698

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Triglycerides to Total Lipids in Large HDL percentage

HIP1R · rs11060344

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Citrate levels

GPR180 · rs6492721

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Average diameter for HDL particles

intergenic · rs2224539

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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.