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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,129 positions on this site are linked to Height, out of 2,506,525 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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 LINC02606 · rs12561781

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Standard

Height

near TMEM161B · rs11948659

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Standard

Height

CHRNE · rs3966782

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Standard

Height

MIR34BHG · rs28690953

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Standard

Height

TSPAN9 · rs41423644

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Standard

Height (baseline)

near EFEMP1 · rs139257983

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Standard

Height (baseline)

near H4C12 · rs13219151

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Standard

Height (baseline)

near H2BC21 · rs79191594

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Standard

Height

TET2 · rs2647257

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Standard

Height

LRRC8C · rs12032393

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Standard

Height (maximum, inv-normal transformed)

CEP120 · rs1047440

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Standard

Standing height (UKB data field 50)

near LINC02817 · rs12025127

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Standard

Height (baseline)

GIGYF2 · rs283468

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Standard

Height

MYL2 · rs7304705

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Standard

Height (baseline)

near KRT18P51 · rs190135380

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Standard

Height (maximum, inv-normal transformed)

near RPL34-DT · rs56120975

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Standard

Height

FBXO32 · rs7835298

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Standard

Height

TRIB1AL · rs12676771

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Standard

Height

MRPS21 · rs12403795

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Standard

Standing height (UKB data field 50)

near RN7SL7P · rs62466110

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Showing 20 of 11129 · page 205 of 557

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.