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)

ST3GAL3 · rs138536153

See detailed info → Standard

Height

CENPP · rs13301537

See detailed info → Standard

Height

UBAP2 · rs13287325

See detailed info → Standard

Height (baseline)

near ANK1 · rs13249022

See detailed info → Standard

Height (baseline)

GMDS · rs13197291

See detailed info → Standard

Height

ATMIN · rs13185

See detailed info → Standard

Height (baseline)

near KLHL5 · rs13128482

See detailed info → Standard

Height

LSAMP · rs13088089

See detailed info → Standard

Height (baseline)

MIR3681HG · rs13022088

See detailed info → Standard

Height (baseline)

near PTH2 · rs12974629

See detailed info → Standard

Height (baseline)

SCAPER · rs12911987

See detailed info → Standard

Height (baseline)

near RPL13AP23 · rs12819172

See detailed info → Standard

Height (standard GWA)

GLI2 · rs12616192

See detailed info → Standard

Height

XYLT1 · rs12596556

See detailed info → Standard

Height

KDM4C · rs12554351

See detailed info → Standard

Height

MICOS10-NBL1 · rs12408388

See detailed info → Standard

Height

SMOC2 · rs1232314

See detailed info → Standard

Height (baseline)

near NACAP2 · rs12259734

See detailed info → Standard

Height (baseline)

LINC02895 · rs12148447

See detailed info → Standard

Height

near AGBL1 · rs12148333

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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.