Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 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 (baseline)

near RNU1-62P · rs74957747

See detailed info → Standard

Height (baseline)

TIAM2 · rs745535

See detailed info → Standard

Height

PCP4 · rs741792

See detailed info → Standard

Height

near GAPDHP31 · rs7313726

See detailed info → Standard

Height (baseline)

near MICALL2 · rs73038811

See detailed info → Standard

Height (baseline)

NFILZ · rs73006466

See detailed info → Standard

Height (baseline)

KCNQ1 · rs72844296

See detailed info → Standard

Height (baseline)

IGF1R · rs72752830

See detailed info → Standard

Height (standard GWA)

near CIBAR1P2 · rs72689854

See detailed info → Standard

Height (standard GWA)

near SPTY2D1 · rs71486871

See detailed info → Standard

Height

VPS37C · rs7116493

See detailed info → Standard

Height

near RHOBTB1 · rs7091284

See detailed info → Standard

Height

near ADRB1 · rs7080638

See detailed info → Standard

Height

near KLHL7-DT · rs6956514

See detailed info → Standard

Height

LINC02615 · rs6815701

See detailed info → Standard

Height (baseline)

KLHL24 · rs6794358

See detailed info → Standard

Height

TRPM6 · rs6560408

See detailed info → Standard

Height

THOC1-DT · rs650695

See detailed info → Standard

Height

SLC9A9 · rs6440170

See detailed info → Standard

Height (baseline)

near BATF2 · rs627880

See detailed info →

Showing 20 of 11479 · page 269 of 574

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.