Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Oct 25, 2026

1,155 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 118,462 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Cholesterol (LDL, HDL and Total)

Standard

Cholesteryl Esters in Small HDL

CREB3L1 · rs7113904

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Free Cholesterol to Total Lipids in IDL percentage

FAM210A · rs180690452

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Omega-3 fatty acids levels

ETV5 · rs1516726

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Phospholipids in small HDL

RABGAP1L · rs12087441

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Cholesteryl esters in very large VLDL

near CEP112 · rs9906319

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Phospholipids in small HDL

near CHCHD7 · rs35205529

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Total lipids in small HDL

GGA3 · rs199641812

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Total lipids in large HDL

near Y_RNA · rs1817649

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Cholesteryl Esters to Total Lipids in Very Large VLDL percentage

CALCB · rs113990148

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Cholesteryl Esters to Total Lipids in Small LDL percentage

near LINC-PINT · rs10245520

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Phospholipids in small HDL

ZFP30 · rs16958861

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Cholesterol to Total Lipids in Medium HDL percentage

LINC01169 · rs4776304

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Free Cholesterol to Total Lipids in Very Large HDL percentage

near SH3KBP1 · rs111876644

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Cholesteryl Esters to Total Lipids in IDL percentage

FOXN3 · rs4904549

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Cholesteryl Esters to Total Lipids in Small VLDL percentage

MAP2K2 · rs2890215

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Phospholipids in small HDL

near PPIF · rs11002939

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Cholesteryl Esters to Total Lipids in Small VLDL percentage

LINC02227 · rs2964481

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Triglycerides to Total Lipids in Very Large HDL percentage

FBXL17 · rs256538

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Free Cholesterol to Total Lipids in Medium HDL percentage

MIR4435-2HG · rs73954926

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Triglycerides to Total Lipids in Large LDL percentage

near GSTT4 · rs12158430

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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.