Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,146 positions on this site are linked to Height, out of 2,506,627 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

FOXP4 · rs912883

See detailed info → Standard

Height

LINC01681 · rs2225588

See detailed info → Standard

Height

near HMGB3P18 · rs9320841

See detailed info → Standard

Height

near RPL34-DT · rs4593211

See detailed info → Standard

Height

near AHNAK · rs3017106

See detailed info → Standard

Height

SIRPA · rs6075340

See detailed info → Standard

Height

AKAIN1 · rs292285

See detailed info → Standard

Height

GLCCI1 · rs2240857

See detailed info → Standard

Height (baseline)

VPS13B · rs1788161

See detailed info → Standard

Height (baseline)

near SMOX · rs34828771

See detailed info → Standard

Height in pregnancy

TRIP11 · rs7155279

See detailed info → Standard

Height

ELL2 · rs11135441

See detailed info → Standard

Height

near FAM53A · rs811316

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

near CYTL1 · rs62291609

See detailed info → Standard

Height

DDC · rs2167364

See detailed info → Standard

Height

near POLR3KP2 · rs2017811

See detailed info → Standard

Height

near MVK · rs1541597

See detailed info → Standard

Height

AK3 · rs12348423

See detailed info → Standard

Height (baseline)

near WNT4 · rs2744716

See detailed info → Standard

Height (maximum, inv-normal transformed)

TWIST2 · rs140091823

See detailed info →

Showing 20 of 11146 · page 214 of 558

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.