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 2,506,525 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

NMT2 · rs10906841

See detailed info → Standard

Height (baseline)

ADAP2 · rs117870634

See detailed info → Standard

Height

TBX15 · rs946210

See detailed info → Standard

Height

UBXN6 · rs760369

See detailed info → Standard

Height (baseline)

STAG1 · rs9809269

See detailed info → Standard

Height

PDE7B · rs2327672

See detailed info → Standard

Height

near MIR4425 · rs12403486

See detailed info → Standard

Height

CTU2 · rs8059048

See detailed info → Standard

Height

DIS3L2 · rs6728302

See detailed info → Standard

Height

SMOC2 · rs2342646

See detailed info → Standard

Height

FMNL1-DT · rs17630064

See detailed info → Standard

Height

AMZ1 · rs798557

See detailed info → Standard

Height

LETR1 · rs12912439

See detailed info → Standard

Height

near CRYAB · rs12808601

See detailed info → Standard

Height

near ATP5MC2 · rs10876470

See detailed info → Standard

Height

ADAMTS17 · rs746711

See detailed info → Standard

Height

near IGFBP4 · rs584828

See detailed info → Standard

Height (baseline)

SPDEF · rs75149985

See detailed info → Standard

Height

TGFB2 · rs1418553

See detailed info → Standard

Height

PPP2R2D · rs9419374

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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.