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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 2,506,771 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

Free Cholesterol to Total Lipids in Medium HDL percentage

MIR4435-2HG · rs73954926

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Total cholesterol levels

BLMH · rs56881390

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Triglycerides to Total Lipids in Large LDL percentage

near GSTT4 · rs12158430

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Cholesterol to Total Lipids in Small HDL percentage

near RNU4-17P · rs79077117

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Free cholesterol in small HDL

SMC4 · rs7631792

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Phospholipids to Total Lipids in Large LDL percentage

near ADRB1 · rs4917675

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Cholesteryl Esters in Small VLDL

DDB2 · rs2596397

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Triglycerides to Total Lipids in Large HDL percentage

GNAI1 · rs10241877

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Total cholesterol levels

XRN1 · rs7642634

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Triglycerides to Total Lipids in Large LDL percentage

SGMS1 · rs61856787

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Total cholesterol levels

GAB2 · rs4945274

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High density lipoprotein cholesterol levels

near LINC-ADAIN · rs4741016

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Free Cholesterol to Total Lipids in Small HDL percentage

VKORC1 · rs2884737

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Total cholesterol levels

near CYSTM1 · rs269781

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Phospholipids to Total Lipids in Small HDL percentage

MANEA · rs13192906

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Phospholipids to Total Lipids in Very Large HDL percentage

VPS11 · rs1185460

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Low density lipoprotein cholesterol levels

TRIM54 · rs7575245

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Total cholesterol levels

RABEP1 · rs145437104

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Phospholipids to Total Lipids in Very Large HDL percentage

FLACC1 · rs1406121

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High density lipoprotein cholesterol levels

near BEAN1 · rs114876144

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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.