Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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

near MRPS30 · rs6891637

See detailed info → Standard

Height (baseline)

RTN4 · rs6545469

See detailed info → Standard

height (mean, inv-normal transformed)

THADA · rs6544650

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Height

near CEPT1 · rs641379

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Height (baseline)

DIRC3 · rs62175472

See detailed info → Standard

Height (baseline)

AKAP13 · rs62024510

See detailed info → Standard

Height (baseline)

NUP50P1 · rs61987039

See detailed info → Standard

Height (baseline)

REST · rs61748757

See detailed info → Standard

Height

near RN7SL547P · rs6038858

See detailed info → Standard

Height

MIR3681HG · rs60261717

See detailed info → Standard

Height (baseline)

DOCK3 · rs59048489

See detailed info → Standard

Height (standard GWA)

near ZNRF3 · rs5752820

See detailed info → Standard

Height (baseline)

BAK1 · rs5745577

See detailed info → Standard

Height (baseline)

AP3D1 · rs55848295

See detailed info → Standard

Height

near PNMA8A · rs4803953

See detailed info → Standard

Height

MYC · rs4645948

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Height

GUSBP5 · rs4513513

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Height (baseline)

near PTPDC1 · rs4260950

See detailed info → Standard

Height

near ESRRG · rs4240923

See detailed info → Standard

height (minimum, inv-normal transformed)

BLM · rs416014

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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.