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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 2,506,525 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

ABCB11 · rs2287621

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Standard

Low density lipoprotein cholesterol levels

near CCDC93 · rs72838078

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Standard

Low density lipoprotein cholesterol levels

EVI5 · rs2027061

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Low density lipoprotein cholesterol levels

VMP1 · rs2645492

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Low density lipoprotein cholesterol levels

IRF1 · rs2522061

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Low density lipoprotein cholesterol levels

OIT3 · rs57176252

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Total cholesterol levels

M6PR · rs1805248

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Standard

Total cholesterol levels

ST3GAL4 · rs59379014

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Low density lipoprotein cholesterol levels

LIMS1 · rs826681

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High density lipoprotein cholesterol levels

PGS1 · rs4969183

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High density lipoprotein cholesterol levels

HECTD4 · rs77768175

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High density lipoprotein cholesterol levels

FRMD5 · rs481837

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High density lipoprotein cholesterol levels

UBE3B · rs10744826

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High density lipoprotein cholesterol levels

UBASH3B · rs7115089

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High density lipoprotein cholesterol levels

UBE3B · rs2241208

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Standard

High density lipoprotein cholesterol levels

near UBASH3B · rs11218720

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High density lipoprotein cholesterol levels

GPAM · rs7096937

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High density lipoprotein cholesterol levels

GPAM · rs2803621

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High density lipoprotein cholesterol levels

GPAM · rs77147124

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High density lipoprotein cholesterol levels

MADD · rs10838692

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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.