Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,616 positions on this site are linked to Height, out of 2,511,293 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

Standing height (UKB data field 50)

ANO1 · rs4411303

See detailed info → Standard

Standing height (UKB data field 50)

SERGEF · rs4393297

See detailed info → Standard

Height

near KIAA0232 · rs4302466

See detailed info → Standard

Height (baseline)

UQCC1 · rs41311302

See detailed info → Standard

Height

TRIM5 · rs3740995

See detailed info → Standard

Height

near RXRA · rs3118545

See detailed info → Standard

Height

near PLD4 · rs2919622

See detailed info → Standard

Height

PDE1A · rs2887208

See detailed info → Standard

Height

TIAM1 · rs2833346

See detailed info → Standard

Height

APP · rs2830088

See detailed info → Standard

Height

ADCY6-DT · rs2446990

See detailed info → Standard

Height

TTC34 · rs2377041

See detailed info → Standard

Height

GAPT · rs2307117

See detailed info → Standard

Height

DDB2 · rs2291120

See detailed info → Standard

Height

DOT1L · rs2286329

See detailed info → Standard

Height

GTF2B · rs2275669

See detailed info → Standard

Height

C1orf21 · rs2207527

See detailed info → Standard

Standing height (UKB data field 50)

STK4 · rs2157363

See detailed info → Standard

Height

ABHD13 · rs2148429

See detailed info → Standard

Height

near RPL12P46 · rs2085833

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Showing 20 of 11616 · page 516 of 581

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.