Gene Knowledge Graph
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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

NXPH1 · rs7802159

See detailed info → Standard

Height (baseline)

TMOD1 · rs77834412

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Height (baseline)

MTREX · rs7737351

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Height (baseline)

near LINC01975 · rs76401897

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Height

near LINC01956 · rs7593247

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Height (baseline)

MIR4432HG · rs7572340

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Height (baseline)

MLF1-DT · rs75672969

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Height (baseline)

near CHCHD7 · rs75192808

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Height (baseline)

LINC02687 · rs7482739

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Height (standard GWA)

near CASC20 · rs74597915

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Height (baseline)

near THBS2-AS1 · rs7450180

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Height (standard GWA)

near FZD9 · rs74366373

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Height (baseline)

LINC02687 · rs74325743

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Height (baseline)

near LINC02120 · rs73759159

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Height (baseline)

ASTN2 · rs73655479

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Height (baseline)

MLXIP · rs73217776

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Height

ADAM22 · rs73202341

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Height (baseline)

FNDC3B · rs73167259

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Height (baseline)

SLC13A4 · rs73160728

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Height

LDHB · rs73079245

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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.