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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

Cholesteryl Esters to Total Lipids in Very Large HDL percentage

CHLSN · rs12701713

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Cholesteryl Esters to Total Lipids in Very Large HDL percentage

PIGU · rs6088559

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Cholesterol esters in very large HDL

WIPI1 · rs67556103

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Cholesterol esters in very large HDL

ETV5 · rs74607912

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Free Cholesterol to Total Lipids in Very Large HDL percentage

RBM6 · rs11925192

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Free Cholesterol to Total Lipids in Very Large HDL percentage

CYP26C1 · rs12263369

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Free Cholesterol to Total Lipids in Very Large HDL percentage

CLCN6 · rs12567119

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Free cholesterol in very large HDL

ABCG5 · rs111617668

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Free cholesterol in very large HDL

DCPS · rs73632723

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Total lipids in very large HDL

FAF1 · rs12354253

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Total lipids in very large HDL

near OR5AS1 · rs12420198

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Total lipids in very large HDL

FDFT1 · rs1497042

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Total lipids in very large HDL

near GIMAP4 · rs56363175

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Concentration of very large HDL particles

near DHODH · rs12934018

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Concentration of very large HDL particles

NPC1 · rs1623060

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Concentration of very large HDL particles

PPARG · rs17036170

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Concentration of very large HDL particles

GCDH · rs1799918

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Concentration of very large HDL particles

near SRGAP2C · rs183174615

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Concentration of very large HDL particles

TTC19 · rs2302415

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Standard

Concentration of very large HDL particles

AMPD3 · rs7111987

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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.