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 8, 2026

10,926 positions on this site are linked to Height, out of 2,505,576 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

OSTN · rs2034771

See detailed info → Standard

Height

near FFAR4 · rs1889931

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Height

RPN2 · rs6130802

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Height

near LINC01876 · rs11898359

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Height

near LINC02563 · rs17746801

See detailed info → Standard

Height

FXR2 · rs34416693

See detailed info → Standard

Height

near ZNF619P1 · rs17151092

See detailed info → Standard

Height (baseline)

LINC02456 · rs143463116

See detailed info → Standard

Height

SLC4A4 · rs4458426

See detailed info → Standard

Height

near MTCO3P1 · rs3873444

See detailed info → Standard

Height

ARHGAP10 · rs2358182

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Height

FBXO11 · rs13430439

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Height

near IFT88 · rs13378757

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Height

SMAD9 · rs9576129

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Height

NACC1 · rs4926210

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Height

near NNT · rs4574552

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Height

FAF1 · rs12078434

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Height

near THRAP3P1 · rs7649423

See detailed info → Standard

Height

near RPL23AP31 · rs730947

See detailed info → Standard

Height

TEKT2 · rs399393

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Showing 20 of 10926 · page 155 of 547

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.