Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,486 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

THSD4 · rs11858418

See detailed info → Standard

Height (baseline)

near SBNO1-AS1 · rs117718416

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Height (baseline)

EML5 · rs117703861

See detailed info → Standard

Height (baseline)

near EFL1 · rs117687334

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Height (baseline)

near RN7SL643P · rs11759530

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Height (baseline)

SSR1 · rs11758313

See detailed info → Standard

Height

IL21R · rs117535117

See detailed info → Standard

Height (standard GWA)

FBXW8 · rs117425351

See detailed info → Standard

Height (baseline)

MFSD1 · rs11721000

See detailed info → Standard

Height (baseline)

LINC02259 · rs117080652

See detailed info → Standard

Height

FAM184B · rs116972792

See detailed info → Standard

Height

WWTR1-AS1 · rs116959924

See detailed info → Standard

Height

near MAP2 · rs11678209

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Height (baseline)

near RNU6-500P · rs116616948

See detailed info → Standard

Height (standard GWA)

SPG7 · rs11645860

See detailed info → Standard

Height (baseline)

near SEPTIN7P14 · rs115914847

See detailed info → Standard

Height (baseline)

near RPTN · rs11582331

See detailed info → Standard

Height

near URB2 · rs11581050

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Height (baseline)

EXOC6B · rs115772341

See detailed info → Standard

Height (baseline)

ZZEF1 · rs115725560

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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.