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 2,506,771 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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Recommended (connected, strongest) Strongest evidence Newest Oldest

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

Total cholesterol levels

SLC44A1 · rs7032034

See detailed info → Standard

Low density lipoprotein cholesterol levels

NDC1 · rs191875604

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Total cholesterol levels

CWF19L1 · rs17668357

See detailed info → Standard

Low density lipoprotein cholesterol levels

LINC01483 · rs75910690

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Total cholesterol levels

LINC01755 · rs148939072

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Cholesterol to Total Lipids in Small LDL percentage

near APOB · rs571468

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Total cholesterol levels

near AREG · rs189087436

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High density lipoprotein cholesterol levels

RNF111 · rs112147665

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Total cholesterol levels

near GC · rs938075289

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Low density lipoprotein cholesterol levels

PLEC · rs11787335

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Phospholipids to Total Lipids in Small HDL percentage

INPP5E · rs13290734

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High density lipoprotein cholesterol levels

CHLSN · rs34409228

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Low density lipoprotein cholesterol levels

TNXB · rs7774197

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High density lipoprotein cholesterol levels

CDH3 · rs564672295

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Low density lipoprotein cholesterol levels

CHLSN · rs10272002

See detailed info → Standard

Low density lipoprotein cholesterol levels

DNAJC13 · rs74341202

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Low density lipoprotein cholesterol levels

LPA · rs190068306

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Low density lipoprotein cholesterol levels

TYK2 · rs12720359

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Low density lipoprotein cholesterol levels

near PDHB · rs71311871

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Glucose levels

near BTBD7P2 · rs10885120

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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.