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

11,668 positions on this site are linked to Height, out of 2,512,045 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 DYM-AS1 · rs736839

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Height

INTS7 · rs2993533

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Height

KBTBD2 · rs17161546

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Height

HNRNPD · rs34471118

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Height

ARSJ · rs11098219

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Height

near LINC02188 · rs12919935

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Height

near PDE5A · rs17051339

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Height

near ATAD2B · rs2551320

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Height

TMEM43 · rs3796308

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Height

TTC7A · rs11125114

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Height

GPR78 · rs9799721

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Height

COL11A1 · rs3767272

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Standing height (UKB data field 50)

DYM · rs11664336

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Height

TOX4 · rs12878084

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Height

near SKOR2 · rs2684853

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Height

near U6 · rs223982

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Height

DOCK9 · rs4772157

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Height

IGF1R · rs1317459

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Height

TENT4A · rs2290616

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Height

ZFAT · rs17778003

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Showing 20 of 11668 · page 49 of 584

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.