Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,493 positions on this site are linked to Height, out of 2,509,702 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)

ZFHX3 · rs77046572

See detailed info → Standard

Height

near GBA3 · rs7689638

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Height (standard GWA)

AFAP1 · rs7689238

See detailed info → Standard

Height

LTBP3 · rs763648441

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Height (baseline)

PVT1 · rs76298623

See detailed info → Standard

Height (standard GWA)

ANTXR1 · rs76216304

See detailed info → Standard

Height

near ATP4B · rs75779304

See detailed info → Standard

Height (standard GWA)

JAZF1-AS1 · rs75685985

See detailed info → Standard

Height

LPIN1 · rs7561070

See detailed info → Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

LINC01732 · rs7550430

See detailed info → Standard

Height

PLCB4 · rs75401168

See detailed info → Standard

Height (baseline)

ITPK1 · rs75036981

See detailed info → Standard

Height (baseline)

near PTHLH · rs74774685

See detailed info → Standard

Height

TNIK · rs7375039

See detailed info → Standard

Height (baseline)

near FAM76B · rs735028

See detailed info → Standard

Height (baseline)

near BOD1L1 · rs73231553

See detailed info → Standard

Height

UBE2N · rs7303274

See detailed info → Standard

Height (baseline)

EBF1 · rs72813940

See detailed info → Standard

Height (baseline)

PRTFDC1 · rs72780342

See detailed info → Standard

Height (baseline)

near C14orf39 · rs72720169

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Showing 20 of 11493 · page 309 of 575

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.