Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 positions on this site are linked to Height, out of 2,509,486 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

HDAC7 · rs12820931

See detailed info → Standard

Height (standard GWA)

near CACHD1 · rs12748897

See detailed info → Standard

Height (standard GWA)

COLGALT2 · rs12725649

See detailed info → Standard

Height

near RNU6-153P · rs12663423

See detailed info → Standard

Height (baseline)

PKD2L2 · rs12656492

See detailed info → Standard

Height (baseline)

PELI2 · rs12589245

See detailed info → Standard

Height

near FGF3 · rs12577891

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Height

KIF9 · rs12495173

See detailed info → Standard

Height

RORA · rs12441507

See detailed info → Standard

Height (baseline)

SMAD3 · rs12438366

See detailed info → Standard

Height

near RPL15P2 · rs1243513

See detailed info → Standard

Height

PPP2R5C · rs12432614

See detailed info → Standard

Height

SLC38A4 · rs12307687

See detailed info → Standard

Height (baseline)

near RPL5P21 · rs12191170

See detailed info → Standard

Height (baseline)

near RNA5SP56 · rs12123373

See detailed info → Standard

Height

near LINC02099 · rs11989810

See detailed info → Standard

Height (baseline)

NMU · rs11933778

See detailed info → Standard

Height (baseline)

near TENT5A · rs118115556

See detailed info → Standard

Height (baseline)

near RNU6-241P · rs117836614

See detailed info → Standard

Height (baseline)

PHF20 · rs117726271

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Showing 20 of 11486 · page 276 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.