Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,696 positions on this site are linked to Height, out of 2,512,461 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)

near DUSP1 · rs34683389

See detailed info → Standard

Height

PPM1H · rs342153

See detailed info → Standard

Height

near SPATA31J1 · rs28833246

See detailed info → Standard

Height

near PRDX4P1 · rs28585622

See detailed info → Standard

Height (baseline)

NOS3 · rs2853792

See detailed info → Standard

Height

RSPH1 · rs2839538

See detailed info → Standard

Height

near ABCG1 · rs2839475

See detailed info → Standard

Height

TSBP1-AS1 · rs28362680

See detailed info → Standard

Height

SETD4 · rs2835269

See detailed info → Standard

Height (baseline)

near EIF1AXP1 · rs2761490

See detailed info → Standard

Height

FOXN3 · rs243183

See detailed info → Standard

Height

near MRPL42P4 · rs2346855

See detailed info → Standard

Height (baseline)

COLEC12 · rs2305029

See detailed info → Standard

Height

TBCD · rs2292969

See detailed info → Standard

Height

near TPT1P9 · rs2244872

See detailed info → Standard

Height (standard GWA)

near LINC01713 · rs2206922

See detailed info → Standard

Height

PDE4D · rs2112956

See detailed info → Standard

Height

near SHISAL1 · rs1974462

See detailed info → Standard

Height

SAMD4A · rs1957356

See detailed info → Standard

Height (baseline)

near TMEM68 · rs190986768

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.