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

11,083 positions on this site are linked to Height, out of 2,506,432 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 HCG15 · rs6904975

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Standard

Height

FLI1 · rs688019

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Standard

Standing height (UKB data field 50)

RGS17 · rs676199

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Standard

Height (baseline)

near LINC01808 · rs6713895

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Standard

Height

NMT1 · rs6503410

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Standard

Height

LINC01483 · rs6501333

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Standard

Height

near ASTILCS · rs56401210

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Standard

Height (baseline)

HLA-DRB5 · rs563205344

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Standard

Height

BCL2 · rs4987852

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Standard

Height

TTYH2 · rs4789047

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Standard

Height

LINC01169 · rs4776305

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Standard

Height

near TOPORSLP · rs4743699

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Standard

Height

near KRBOX5P1 · rs4479245

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Standard

Height

near RPS23P4 · rs4373182

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Standard

Height

near LSM3 · rs4355260

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Standard

Height

near RNA5SP431 · rs4243170

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Standard

Height

TNPO1-DT · rs3916720

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Standard

Height

IGF2R · rs3798176

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Standard

Height

TNRC6C · rs3764379

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Standard

Height

PRRG2 · rs3760706

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Showing 20 of 11083 · page 387 of 555

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.