Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,696 positions on this site are linked to Height, out of 2,512,461 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 FGFR4 · rs187259907

See detailed info → Standard

Height

near RNA5SP225 · rs1843691

See detailed info → Standard

Height

RORA · rs1816624

See detailed info → Standard

Height

LINC02288 · rs17811461

See detailed info → Standard

Height

near RNU4ATAC9P · rs17779822

See detailed info → Standard

Height

TESHL · rs17773051

See detailed info → Standard

Height

LINC-PINT · rs17688449

See detailed info → Standard

Height

IFNGR2 · rs17644622

See detailed info → Standard

Height

BNIP3L · rs17310286

See detailed info → Standard

Height (baseline)

near RNF39 · rs17187735

See detailed info → Standard

Height

LINC02319 · rs17125121

See detailed info → Standard

Height

LINC01389 · rs17103227

See detailed info → Standard

Height

ZRANB2-DT · rs17097556

See detailed info → Standard

Height

near PAPOLA · rs17094171

See detailed info → Standard

Height

near RPS27P4 · rs17050944

See detailed info → Standard

Height

LINC01726 · rs16982885

See detailed info → Standard

Height

RPL37A · rs16856373

See detailed info → Standard

Height

near ZBTB8OSP2 · rs16828053

See detailed info → Standard

Height (baseline)

TMEM241 · rs1501411

See detailed info → Standard

Height (baseline)

near SFMBT1 · rs149415292

See detailed info →

Showing 20 of 11696 · page 364 of 585

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.