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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

High density lipoprotein cholesterol levels

DAGLB · rs79949326

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Standard

High density lipoprotein cholesterol levels

AKT1 · rs2494747

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Standard

Low density lipoprotein cholesterol levels

near HNRNPA1P55 · rs181372486

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Low density lipoprotein cholesterol levels

OSGIN1 · rs67890964

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High density lipoprotein cholesterol levels

near UBASH3B · rs6589939

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Standard

Total cholesterol levels

near RPL12P2 · rs4714035

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LDL cholesterol

near MTCO3P1 · rs13205804

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Total cholesterol levels

TRIM59-IFT80 · rs4679881

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Standard

Low density lipoprotein cholesterol levels

ZNF404 · rs76989105

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Phospholipids to Total Lipids in Small HDL percentage

near MIR4424 · rs1074896

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High density lipoprotein cholesterol levels

CCDC102A · rs12924311

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Low density lipoprotein cholesterol levels

EVI5 · rs114138180

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Low density lipoprotein cholesterol levels

near RN7SL140P · rs79279183

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High density lipoprotein cholesterol levels

CDH1 · rs571298027

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Average diameter for LDL particles

CMIP · rs56793457

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Cholesterol to Total Lipids in Very Large HDL percentage

near RN7SL140P · rs11693335

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Free Cholesterol to Total Lipids in IDL percentage

near HLA-B · rs34733406

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Low density lipoprotein cholesterol levels

LINC01755 · rs553729354

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Standard

HDL cholesterol

near HLA-B · rs6908001

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Standard

LDL cholesterol

near HLA-DRB5 · rs33997707

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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.