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Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Nov 9, 2026

1,540 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,507,788 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

PPP1R3B-DT · rs34025891

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Standard

HDL cholesterol

THRB · rs2044753

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Standard

LDL cholesterol

near LITAF · rs34318965

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Standard

LDL cholesterol

COG5 · rs2712199

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Standard

HDL cholesterol

near OR10AK1P · rs1011298282

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Standard

High density lipoprotein cholesterol levels

ZFPM2 · rs2941657

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Standard

Total cholesterol levels

ZNF627 · rs192190506

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Standard

High density lipoprotein cholesterol levels

FAM81A · rs187359403

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Standard

HDL cholesterol

IGHVII-33-1 · rs114529226

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Standard

Total cholesterol levels

near VAC14 · rs79252074

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Standard

Low density lipoprotein cholesterol levels

FOXN3 · rs35802157

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LDL cholesterol

TNFAIP1 · rs3093679

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Standard

Low density lipoprotein cholesterol levels

SBNO2 · rs4807570

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Standard

High density lipoprotein cholesterol levels

THRB · rs2044754

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Standard

HDL cholesterol

RIPOR1 · rs183208454

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Standard

High density lipoprotein cholesterol levels

near ATXN1-AS1 · rs1240811

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Standard

HDL cholesterol

near CYCSP42 · rs9978541

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Standard

Low density lipoprotein cholesterol levels

LASP1 · rs640306

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Standard

Low density lipoprotein cholesterol levels

DGKZ · rs61882680

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Standard

HDL cholesterol

near KRT8P37 · rs4749779

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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.