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Variants linked to Cholesterol (LDL, HDL and Total)

Continuously updated · newest added Nov 9, 2026

1,540 positions on this site are linked to Cholesterol (LDL, HDL and Total), out of 2,509,091 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

Total lipids in very large HDL

VMP1 · rs11079389

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Standard

Total lipids in very large HDL

near ZNF644 · rs11582273

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Standard

Total lipids in very large HDL

near RREB1 · rs11759008

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Standard

Total lipids in very large HDL

CHN2 · rs13227449

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Standard

Total lipids in very large HDL

HYOU1 · rs501351

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Standard

Total lipids in very large HDL

NLGN1 · rs583514

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Standard

Total lipids in very large HDL

TNRC6A · rs7202252

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Standard

Total lipids in very large HDL

BIRC6 · rs72785601

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Standard

Total lipids in very large HDL

near QKI · rs73029270

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Standard

Total lipids in very large HDL

near LCORL · rs7696532

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Standard

Total lipids in very large HDL

SCAP · rs77481436

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Standard

Concentration of very large HDL particles

DDX17 · rs138457

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Standard

Concentration of very large HDL particles

near OTOL1 · rs28802383

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Standard

Concentration of very large HDL particles

near ZBTB42 · rs45490496

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Standard

Concentration of very large HDL particles

TGM2 · rs4811528

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Standard

Concentration of very large HDL particles

near ADRB1 · rs7079542

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Standard

Concentration of very large HDL particles

BANP · rs7184826

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Standard

Concentration of very large HDL particles

CTSB · rs7819276

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Standard

Concentration of very large HDL particles

near GBE1 · rs9841087

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Standard

Phospholipids to Total Lipids in Very Large HDL percentage

IRF1 · rs2522062

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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.