Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,493 positions on this site are linked to Height, out of 2,509,608 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

PRKG1 · rs4086289

See detailed info → Standard

Height (baseline)

near LINC02956 · rs4077335

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Height (baseline)

PACSIN1 · rs3857562

See detailed info → Standard

Height

MSH2 · rs3814360

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Height

HRC · rs3745299

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Height (baseline)

near DAP-DT · rs35923197

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Height

EPHA7 · rs345713

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Height (baseline)

near EIF4A1P3 · rs3012765

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Height

near FAF2 · rs2913732

See detailed info → Standard

Height (baseline)

IGF1R · rs28401726

See detailed info → Standard

Height (standard GWA)

near BANF2 · rs2618630

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Height

near RGS6 · rs2526899

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Height

HAO1 · rs2294305

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Height

TM9SF4 · rs2281361

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Height

TASOR2 · rs2275774

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Height

IL1RAPL2 · rs2213321

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Height

near THSD7A · rs2192735

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Height (baseline)

PAH · rs2133295

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Height (baseline)

near CCDC85A · rs191787841

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Height (baseline)

NMU · rs1906677

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Showing 20 of 11493 · page 303 of 575

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.