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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

near NRP1 · rs12358424

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Standard

LDL cholesterol

FER1L4 · rs1010759

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Standard

High density lipoprotein cholesterol levels

SBNO1 · rs10082867

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Cholesteryl Esters to Total Lipids in Large HDL percentage

CCDC162P · rs62436601

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Phospholipids to Total Lipids in Small HDL percentage

PEMT · rs4646392

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Standard

LDL cholesterol

near PLG · rs181711349

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Standard

High density lipoprotein cholesterol levels

near EIF4EP4 · rs74705598

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Standard

High density lipoprotein cholesterol levels

near HLA-DRB9 · rs17209803

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Standard

High density lipoprotein cholesterol levels

near PCIF1 · rs111859808

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High density lipoprotein cholesterol levels

COL18A1 · rs9976784

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Cholesterol in Large HDL

near RGS17 · rs635023

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HDL cholesterol

CPT1A · rs11228374

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Standard

High density lipoprotein cholesterol levels

near FRK · rs1338668

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Low density lipoprotein cholesterol levels

SPRY4-AS1 · rs11167778

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Standard

Triglycerides to Total Lipids in Very Large VLDL percentage

FAF1 · rs72900903

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Standard

High density lipoprotein cholesterol levels

LPA · rs35499210

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Standard

High density lipoprotein cholesterol levels

near ADH5 · rs547953616

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High density lipoprotein cholesterol levels

PDGFC · rs1425485

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Phospholipids to Total Lipids in Small HDL percentage

near DHODH · rs12933886

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Standard

Phospholipids to Total Lipids in Large VLDL percentage

IDUA · rs3796621

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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.