Gene Knowledge Graph
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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 2,506,432 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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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

Cholesterol, total

near RELB · rs34827707

See detailed info → Standard

Cholesterol, total

HLA-C · rs9357121

See detailed info → Standard

Cholesterol, total

PCSK9 · rs7525649

See detailed info → Standard

HDL cholesterol levels

LIPG · rs3786247

See detailed info → Standard

HDL cholesterol levels

MYL2 · rs2188380

See detailed info → Standard

HDL cholesterol

SEMA3C · rs60839105

See detailed info → Standard

Cholesterol, total

NCAN · rs2238675

See detailed info → Standard

Cholesterol, total

KANK2 · rs138534124

See detailed info → Standard

HDL cholesterol

TMEM176A · rs17173637

See detailed info → Standard

LDL cholesterol

EHBP1 · rs2710642

See detailed info → Standard

LDL cholesterol

FN1 · rs1250229

See detailed info → Standard

LDL cholesterol

APOB · rs12713956

See detailed info → Standard

LDL cholesterol

PPARG · rs2920503

See detailed info → Standard

LDL cholesterol

ST3GAL4 · rs4307732

See detailed info → Standard

LDL cholesterol

SNX5 · rs2618568

See detailed info → Standard

LDL cholesterol

FAM117B · rs140244541

See detailed info → Standard

Cholesterol, total

DLG4 · rs314253

See detailed info → Standard

Cholesterol, total

HBS1L · rs9376090

See detailed info → Standard

Cholesterol, total

GPR146 · rs1997243

See detailed info → Standard

Cholesterol, total

ERGIC3 · rs2277862

See detailed info →

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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.