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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

Phospholipids to Total Lipids in Small VLDL percentage

DNAH1 · rs390802

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Standard

Triglycerides to Total Lipids in Small VLDL percentage

RIC8B · rs10861662

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Standard

Total cholesterol levels

REEP3 · rs7898861

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Standard

Total cholesterol levels

near HLA-DQA1 · rs28383323

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Standard

Total esterified cholesterol levels

LILRB5 · rs11668189

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Standard

Total concentration of lipoprotein particles

MIDEAS · rs11627539

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Standard

Total concentration of lipoprotein particles

near PCSK6 · rs8025505

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Standard

Total phospholipid levels in lipoprotein particles

near RAPSN · rs35184771

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Standard

Tyrosine levels

near CDKN2B · rs10217762

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Standard

Tyrosine levels

near MAF · rs17689625

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Standard

Degree of unsaturation

AGPAT2 · rs9411215

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Standard

Valine levels

WDR20 · rs12883945

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Standard

Valine levels

GTF2H1 · rs4150581

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Standard

Valine levels

SLC38A4 · rs79020793

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Standard

Triglycerides in VLDL

GCK · rs2908297

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Standard

Cholesterol to Total Lipids in Very Large HDL percentage

GBF1 · rs17780834

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Standard

Cholesterol to Total Lipids in Very Large HDL percentage

near GPIHBP1 · rs60987469

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Standard

Cholesterol to Total Lipids in Very Large HDL percentage

near LPL · rs74615535

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Standard

Cholesterol levels in very large HDL

MST1R · rs2280406

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Standard

Cholesterol levels in very large HDL

VMP1 · rs2665403

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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.