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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 2,506,432 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

Cholesterol to Total Lipids in Small LDL percentage

near RP1L1 · rs60410697

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Standard

Total cholesterol levels

LINC00466 · rs574313788

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Standard

Free Cholesterol to Total Lipids in Large VLDL percentage

near GRB7 · rs9747973

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Standard

Low density lipoprotein cholesterol levels

LNROP · rs562494568

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Standard

Free Cholesterol to Total Lipids in Large VLDL percentage

near TRIM48 · rs74966104

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Standard

Low density lipoprotein cholesterol levels

near GSTM5 · rs140266316

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Standard

Low density lipoprotein cholesterol levels

LIPE-AS1 · rs538657595

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Standard

Cholesterol, total

MTHFD2L · rs182616603

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Cholesteryl Esters in Small HDL

near SEC24B · rs114053844

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Standard

Citrate levels

COQ10A · rs11543260

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Standard

Cholesterol to Total Lipids in Small VLDL percentage

near NOLC1 · rs17779355

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Triglycerides in very large VLDL

PPARG · rs35000407

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Low density lipoprotein cholesterol levels

near Y_RNA · rs139262716

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Standard

Low density lipoprotein cholesterol levels

RAB10 · rs142787485

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Standard

High density lipoprotein cholesterol levels

near TMEM106B · rs1990622

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Standard

Free Cholesterol to Total Lipids in Small LDL percentage

RNFT2 · rs3809192

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Standard

Cholesterol in Small HDL

near GSTT2B · rs575146

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Standard

Total cholesterol levels

near U8 · rs11576986

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LDL cholesterol

C7orf50 · rs10275712

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Standard

High density lipoprotein cholesterol levels

SH3YL1 · rs17713729

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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.