Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,464 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

KDM2B · rs147903411

See detailed info → Standard

Height

SNX24 · rs1478417

See detailed info → Standard

Height (baseline)

NSF · rs147405729

See detailed info → Standard

Height (baseline)

AMZ1 · rs146838251

See detailed info → Standard

Height (baseline)

SLC12A2-DT · rs146579248

See detailed info → Standard

Height (baseline)

near CENPW · rs146096428

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Height (baseline)

near RSPO3 · rs144948316

See detailed info → Standard

Height

near FAT3 · rs143094021

See detailed info → Standard

Height (baseline)

near SH3GL3 · rs141795224

See detailed info → Standard

Height (baseline)

RRP15 · rs141714452

See detailed info → Standard

Height (baseline)

PSMD9 · rs141559222

See detailed info → Standard

Height (baseline)

UBE2Q2P1 · rs141288982

See detailed info → Standard

Height (baseline)

near LINC02009 · rs140301305

See detailed info → Standard

Height (baseline)

SPON1 · rs139565206

See detailed info → Standard

Height (baseline)

FIG4 · rs139554982

See detailed info → Standard

Height (baseline)

DIRC3 · rs139264983

See detailed info → Standard

Height (baseline)

near RPL35P4 · rs13438221

See detailed info → Standard

Height (baseline)

near LINC02860 · rs13222988

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Height (baseline)

RAB3C · rs13176234

See detailed info → Standard

Height (baseline)

ADAMTS3 · rs13132401

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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.