Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, 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 Height

Standard

Height (baseline)

RPSAP52 · rs537950543

See detailed info → Standard

Height

DOCK3 · rs2306431

See detailed info → Standard

Height

NPFFR1 · rs3812696

See detailed info → Standard

Height

near TLK1 · rs12151587

See detailed info → Standard

Standing height (UKB data field 50)

AKAP13 · rs8033427

See detailed info → Standard

Height (baseline)

PNPLA1 · rs184075118

See detailed info → Standard

Height

LTBP1 · rs12620839

See detailed info → Standard

Height

STON2 · rs11628716

See detailed info → Standard

Height (baseline)

SSH2 · rs113059482

See detailed info → Standard

Height

FER · rs112668446

See detailed info → Standard

Height

HDAC9 · rs6958814

See detailed info → Standard

Height

COL2A1 · rs57444859

See detailed info → Standard

Height

near CFAP65 · rs16859497

See detailed info → Standard

Height

near LINC02527 · rs12663744

See detailed info → Standard

Height

SP7 · rs199673881

See detailed info → Standard

Height

near ADAMTS3 · rs55854248

See detailed info → Standard

Height

COL6A5 · rs4688801

See detailed info → Standard

Height

MRC2 · rs2014055

See detailed info → Standard

Height (baseline)

near ANAPC10 · rs114364021

See detailed info → Standard

Standing height (UKB data field 50)

near H19 · rs74764171

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.