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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

near C8B · rs754633424

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Standard

LDL cholesterol

DOK7 · rs62275880

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Standard

Low density lipoprotein cholesterol levels

RPH3A · rs11066412

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Standard

Low density lipoprotein cholesterol levels

ZNF627 · rs552638138

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Standard

Low density lipoprotein cholesterol levels

near TGDS · rs7330899

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Standard

Low density lipoprotein cholesterol levels

NACC1 · rs560788989

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Free Cholesterol to Total Lipids in Very Large HDL percentage

BDNF-AS · rs11500197

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Standard

Low density lipoprotein cholesterol levels

OSBPL9 · rs570553136

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Standard

Low density lipoprotein cholesterol levels

near NPAS4 · rs117777720

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Low density lipoprotein cholesterol levels

TBC1D8 · rs10185855

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HDL cholesterol

near BDNF · rs12288512

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Total cholesterol levels

near RN7SKP27 · rs557901815

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High density lipoprotein cholesterol levels

PPARG · rs12633551

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LDL cholesterol

TMPRSS11E · rs976058

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High density lipoprotein cholesterol levels

AFF1 · rs342469

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Free Cholesterol to Total Lipids in Very Large VLDL percentage

RMI1 · rs296889

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Standard

Low density lipoprotein cholesterol levels

LY96 · rs62509311

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Standard

Low density lipoprotein cholesterol levels

LINC01344 · rs1689801

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Standard

Low density lipoprotein cholesterol levels

SCAF4 · rs2833487

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Standard

Total cholesterol levels

near LINC01822 · rs2194562

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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.