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

11,272 positions on this site are linked to Height, out of 2,507,647 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

TRIM6-TRIM34 · rs3751006

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Standard

height (minimum, inv-normal transformed)

near TRIP11 · rs67015182

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Standard

Height

EGR3-AS1 · rs2313167

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Standard

Height

ANKRD52 · rs72648137

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Standard

height (minimum, inv-normal transformed)

FLI1 · rs612282

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Standard

Height (baseline)

CASC20 · rs6117293

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Standard

Height

near MIR548A1HG · rs17629312

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Standard

Height

HHIP · rs1355601

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Standard

Height

LHPP · rs10794146

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Standard

Height

LY75 · rs2042772

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Standard

Height

SMG6 · rs1885987

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Standard

Height

USP34 · rs778160

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Standard

Height

DLEU1 · rs9535499

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Standard

Height

PRR16 · rs1404300

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Standard

Height

MKLN1 · rs10954312

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Standard

Height

PDE10A · rs221730

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Standard

Height

FNDC3B · rs1039027

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Standard

Height

CDKN2B-AS1 · rs944802

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Standard

Height

near U3 · rs916893

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Standard

Height

CYP19A1 · rs2445761

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Showing 20 of 11272 · page 562 of 564

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.