Gene Knowledge Graph
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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.

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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

LINC01830 · rs541138574

See detailed info → Standard

Total lipids in small HDL

SESN2 · rs503048

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Free Cholesterol to Total Lipids in Large VLDL percentage

C4orf17 · rs7688705

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Cholesteryl Esters to Total Lipids in Very Large VLDL percentage

GCK · rs35670475

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Total cholesterol levels

near NR1H4 · rs11837065

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Cholesterol in Small HDL

MIDEAS · rs2159176

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High density lipoprotein cholesterol levels

CEP164 · rs74351220

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HDL cholesterol

SULF2 · rs2281279

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Total cholesterol levels

ZNF737 · rs187551406

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Total cholesterol levels

near FBRSL1 · rs75588192

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Total cholesterol levels

near AMBN · rs530082542

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Total cholesterol levels

near RNU6-210P · rs188015971

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Cholesterol to Total Lipids in Small HDL percentage

MIR4435-2HG · rs2165107

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Total cholesterol levels

N4BP2L1 · rs151330264

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Low density lipoprotein cholesterol levels

HELZ · rs9332408

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HDL cholesterol

near HLA-DRB9 · rs78279385

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Low density lipoprotein cholesterol levels

CDKN2B-AS1 · rs10757273

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Triglycerides to Total Lipids in Small HDL percentage

ERBB2 · rs4252627

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Low density lipoprotein cholesterol levels

LRRK2-DT · rs11175540

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Triglycerides to Total Lipids in Very Small VLDL percentage

near RNU4-17P · rs68033110

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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.