Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,607 positions on this site are linked to Height, out of 2,511,197 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

PLPP3 · rs2065554

See detailed info → Standard

Height

SYNM-AS1 · rs2016873

See detailed info → Standard

Height

CCDC158 · rs1876535

See detailed info → Standard

Height (baseline)

near RN7SKP106 · rs1840096

See detailed info → Standard

Height

LPP · rs17669928

See detailed info → Standard

Height

ZSCAN2-AS1 · rs17597517

See detailed info → Standard

Height

ZFHX4 · rs17364641

See detailed info → Standard

Height

near HMGN1P19 · rs17172708

See detailed info → Standard

Height

BMPR1B · rs17022496

See detailed info → Standard

Height

AKAP13 · rs16943484

See detailed info → Standard

Height (baseline)

PTH1R · rs144645644

See detailed info → Standard

Height

PAMR1 · rs1400492

See detailed info → Standard

Height

CHSY3 · rs13356198

See detailed info → Standard

Height

near TAFA1 · rs13315657

See detailed info → Standard

Height

near RPS11P1 · rs12624466

See detailed info → Standard

Height (baseline)

ESR1 · rs12212176

See detailed info → Standard

Height (baseline)

TNRC18 · rs112915601

See detailed info → Standard

Height (baseline)

MTMR9LP · rs111240679

See detailed info → Standard

Height

MAPK8 · rs11101314

See detailed info → Standard

Height

TRIP10 · rs1049232

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.