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Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Nov 9, 2026

1,538 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,507,630 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

AGPAT4 · rs147829643

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Standard

HDL cholesterol

near METAP2P1 · rs13396091

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Standard

LDL cholesterol

COX16 · rs12588332

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Standard

Total cholesterol levels

SLC19A1 · rs9977637

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Standard

LDL cholesterol

PHC1 · rs11048036

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Standard

LDL cholesterol

near APOA4 · rs145859971

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Standard

HDL cholesterol

EYA3 · rs11247731

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Standard

Low density lipoprotein cholesterol levels

APOL3 · rs132646

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Standard

Low density lipoprotein cholesterol levels

near LINC00954 · rs10184466

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Standard

HDL cholesterol

TSPAN16 · rs56121005

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Standard

Low density lipoprotein cholesterol levels

TMEM212-AS1 · rs56118251

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Standard

High density lipoprotein cholesterol levels

LINC01505 · rs535372564

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Standard

High density lipoprotein cholesterol levels

near RRAGC-DT · rs4660446

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Standard

High density lipoprotein cholesterol levels

near DRAIC · rs77648222

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Standard

High density lipoprotein cholesterol levels

near COX4I2 · rs7266471

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Standard

Low density lipoprotein cholesterol levels

ASCC2 · rs5752963

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Standard

High density lipoprotein cholesterol levels

near CES1P1 · rs532566544

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Standard

HDL cholesterol

EDEM2 · rs3746428

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Standard

High density lipoprotein cholesterol levels

PLXND1 · rs2811468

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Standard

High density lipoprotein cholesterol levels

STAT5B · rs180705493

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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.