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 9, 2026

11,344 positions on this site are linked to Height, out of 2,508,253 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 RNU7-167P · rs5750089

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Standard

Height

RP11-513I15.6 · rs1759637

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Standard

Height

GRB10 · rs2715094

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height (mean, inv-normal transformed)

WWP2 · rs11641521

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Standard

Height

ZNF638 · rs4852777

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height (minimum, inv-normal transformed)

near PSPHP1 · rs10232851

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Standing height (UKB data field 50)

PREX1 · rs2664521

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Height (maximum, inv-normal transformed)

EML4 · rs10200353

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Height (baseline)

DGKH · rs9533031

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Height

PTPN14 · rs4472734

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Height

near TRIP11 · rs10129429

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Standing height (UKB data field 50)

ARID5B · rs4245596

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Height

near MAP2K2 · rs350818

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Height

SLC7A1 · rs61947180

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height (mean, inv-normal transformed)

GLCCI1 · rs37983

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Standard

Height

SMIM29-AS1 · rs9469762

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Height

FOXN2 · rs76154567

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Height

near UNCX · rs58063923

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Height

SMURF1 · rs12531875

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Height

near TACC3 · rs28528964

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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.