Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 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

BCAR1 · rs36097424

See detailed info → Standard

Height (baseline)

HIVEP3 · rs35842961

See detailed info → Standard

Height (baseline)

near MPHOSPH6-DT · rs35812977

See detailed info → Standard

Height (standard GWA)

SMAD3-DT · rs35503745

See detailed info → Standard

Height (baseline)

CABLES1 · rs35442828

See detailed info → Standard

Height (baseline)

VPS8 · rs34465973

See detailed info → Standard

Height (standard GWA)

ZBTB42 · rs34284721

See detailed info → Standard

Height

CDK9 · rs3217750

See detailed info → Standard

Height (standard GWA)

near POU1F1 · rs300982

See detailed info → Standard

Height (baseline)

AGO2 · rs2977479

See detailed info → Standard

Height

near KLHL25 · rs2937952

See detailed info → Standard

Height

BMP2K · rs28881880

See detailed info → Standard

Height

CYP19A1 · rs28757082

See detailed info → Standard

Height (baseline)

LINC01418 · rs28463783

See detailed info → Standard

Height

PTCH1 · rs28442014

See detailed info → Standard

Height

near RPS26P29 · rs2757608

See detailed info → Standard

Height (baseline)

near IRF1 · rs2706394

See detailed info → Standard

Height (baseline)

MIR4280HG · rs2624165

See detailed info → Standard

Height (baseline)

PCSK6 · rs2412069

See detailed info → Standard

Height

near CYBRD1 · rs2356791

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Showing 20 of 11486 · page 272 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.