Gene Knowledge Graph
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Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,526 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

LTBP1 · rs1545550

See detailed info → Standard

Height

TET1 · rs12221107

See detailed info → Standard

Height

GLCCI1 · rs10253861

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Height

SPC25 · rs488621

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Height

near HDAC11 · rs2597513

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Height

near ATP13A2 · rs9435734

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Height

PKN2 · rs9428015

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Height

BCKDHB · rs6931421

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Height

near SMIM23 · rs33852

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Height

DNM3 · rs17361789

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Height

AP3D1 · rs1074047

See detailed info → Standard

height (mean, inv-normal transformed)

SLFNL1-AS1 · rs61780439

See detailed info → Standard

height (mean, inv-normal transformed)

near MED6P1 · rs662115

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Height

LCORL · rs925098

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Height (maximum, inv-normal transformed)

CLASP2 · rs151109287

See detailed info → Standard

Height

CALCOCO2 · rs550510

See detailed info → Standard

Height

TENT2 · rs7712162

See detailed info → Standard

Height

TGFB2 · rs10482795

See detailed info → Standard

height (mean, inv-normal transformed)

GNA12 · rs35957220

See detailed info → Standard

Height

FRZB · rs1561369

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Showing 20 of 11639 · page 23 of 582

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.