Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

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.

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

LDL cholesterol

LPA · rs1564348

See detailed info →
Standard

HDL cholesterol

COBLL1 · rs12328675

See detailed info →
Standard

LDL cholesterol

ST3GAL4 · rs11220462

See detailed info →
Standard

Response to statin therapy

FLJ45244 · rs8014194

See detailed info →
Standard

Cholesterol, total

FRK · rs9488822

See detailed info →
Standard

Cholesterol, total

TMEM57 · rs12027135

See detailed info →
Standard

HDL cholesterol

MC4R · rs12967135

See detailed info →
Standard

HDL cholesterol

C6orf106 · rs2814944

See detailed info →
Standard

Cholesterol, total

FAM117B · rs115400054

See detailed info →
Standard

Cholesterol, total

HLA-area · rs114067101

See detailed info →
Standard

HDL cholesterol

LCAT · rs2271293

See detailed info →
Standard

HDL cholesterol

ANGPTL4 · rs7255436

See detailed info →
Standard

HDL cholesterol

UBE2L3 · rs181362

See detailed info →
Standard

HDL cholesterol

LPA · rs1084651

See detailed info →
Standard

HDL cholesterol

ZNF648 · rs1689800

See detailed info →
Standard

HDL cholesterol

STARD3 · rs11869286

See detailed info →
Standard

Cholesterol, total

TMEM57 · rs10903129

See detailed info →
Standard

Response to statin therapy

LOC646909 · rs10091038

See detailed info →

Showing 18 of 1538 · page 77 of 77

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.