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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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

CYP19A1 · rs28566535

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Standard

Height

MEF2C · rs10037512

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Standard

Height

ADAMTSL3 · rs8024628

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Standard

Height

near CTDSP2 · rs10747787

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Standard

Height

near FGFR1 · rs881301

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Standard

height (mean, inv-normal transformed)

CHD4 · rs7310535

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Standard

Height

FGFR4 · rs422421

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Standard

Height

AMZ1 · rs798491

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Standard

Height

ANKS1A · rs13210323

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Standard

Height

HOXD3 · rs4972504

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Standard

Height

near ADAMTS3 · rs4694504

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Standard

Height

C14orf39 · rs1254276

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Standard

Height

MKL2 · rs1659127

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Standard

Height

HMGA1 · rs10807138

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Standard

Height

PPP1CA · rs61734601

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Standard

Facial morphology (factor 9, facial height related to vertical position of nasion)

PARK2 · rs9456748

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Standard

Height

ZBTB21 · rs915837

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Standard

Height

SLC27A2 · rs8032718

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Standard

Height (baseline)

DENND1A · rs79565874

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Standard

Height

RNF207 · rs79344881

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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.