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 10, 2026

11,452 positions on this site are linked to Height, out of 2,509,249 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

NCL · rs997400

See detailed info → Standard

Height

LINC01829 · rs2902005

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Height

FTO · rs12918495

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Standing height (UKB data field 50)

RBPMS · rs6996887

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Height

MBNL1 · rs385685

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Height (baseline)

near NPR3 · rs114794137

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Height (baseline)

near FBN1 · rs79943855

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Height

CCDC3 · rs61852237

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Height (standard GWA)

near SDHB · rs2647166

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height (mean, inv-normal transformed)

FAM118A · rs6007592

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Height (baseline)

near ISLR · rs4886574

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Height

IGF2 · rs3213223

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Height

GNA12 · rs7777484

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Height

INSR · rs7251963

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Height

TRIP11 · rs7158300

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Height

IL18RAP · rs3755266

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Height

near MN1 · rs11913308

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Height (baseline)

CLIP1 · rs10773088

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Height (baseline)

ACAN · rs113238597

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Standing height (UKB data field 50)

LAMC1 · rs10797816

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Showing 20 of 11452 · page 571 of 573

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.