Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,504 positions on this site are linked to Height, out of 2,509,702 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 LINC01012 · rs182056822

See detailed info → Standard

Height (baseline)

RASGEF1C · rs181438167

See detailed info → Standard

Height

near IRAK1BP1 · rs1782783

See detailed info → Standard

Height (baseline)

near SPRY4 · rs17649655

See detailed info → Standard

Height (standard GWA)

PPIL6 · rs17534632

See detailed info → Standard

Height

LINC02240 · rs17465113

See detailed info → Standard

Height

near BOLA2P3 · rs1744849

See detailed info → Standard

Height

near SH3GL3 · rs17158970

See detailed info → Standard

Height

ABCB4 · rs17149674

See detailed info → Standard

Height

near LINC00865 · rs17127699

See detailed info → Standard

Height

SPRY4-AS1 · rs17099100

See detailed info → Standard

Height

PHLPP1 · rs17070418

See detailed info → Standard

Height

near PREP · rs17054938

See detailed info → Standard

Height

AKAP13 · rs16943075

See detailed info → Standard

Height

near KCNE4 · rs16864356

See detailed info → Standard

Height (baseline)

NUMB · rs150563740

See detailed info → Standard

Height (weighted GWA)

THRB · rs1505289

See detailed info → Standard

Height (baseline)

FRS2 · rs149518362

See detailed info → Standard

Height (baseline)

ZMIZ1 · rs148877270

See detailed info → Standard

Height (standard GWA)

SEH1L · rs1474043

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Showing 20 of 11504 · page 314 of 576

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.