Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 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 (baseline)

LINC01512 · rs2182380

See detailed info → Standard

Height (standard GWA)

near ADAMTS17 · rs2082859

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Height

JAK2 · rs202237966

See detailed info → Standard

Height (baseline)

near MIR525 · rs1989486

See detailed info → Standard

Height (baseline)

PPP1R3B-DT · rs17656786

See detailed info → Standard

Height

STXBP3 · rs1759480

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Height

NOC3L · rs17517578

See detailed info → Standard

Height

L3MBTL4 · rs16949431

See detailed info → Standard

Abdominal adipose tissue volumes (adjusted for BMI and height)

near CPA1 · rs1558919

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Height (baseline)

ZCCHC24 · rs149914805

See detailed info → Standard

Height (baseline)

near FAM210B · rs149570493

See detailed info → Standard

Height (baseline)

TRERNA1 · rs146069538

See detailed info → Standard

Height (baseline)

SMIM24 · rs145723843

See detailed info → Standard

Height (baseline)

near RAB11FIP4 · rs141153629

See detailed info → Standard

Height (baseline)

near GPIHBP1 · rs13276096

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Height

TENM2 · rs13177293

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Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

DLG1 · rs13099700

See detailed info → Standard

Height

SLC8A1 · rs13034467

See detailed info → Standard

Height (baseline)

LINC01226 · rs12755649

See detailed info → Standard

Height

LNX1 · rs12642437

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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.