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

SLC38A4-AS1 · rs2287471

See detailed info → Standard

Height

PDE9A · rs2284965

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Height

near LINC00494 · rs226832

See detailed info → Standard

Height

ANKRD36BP1 · rs2205697

See detailed info → Standard

Height

DCBLD2 · rs2119188

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Height (baseline)

near ID4 · rs2056954

See detailed info → Standard

Height at take-off

near CCL27 · rs2026118

See detailed info → Standard

Height

BIVM · rs2018836

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Height (baseline)

RAPGEF6 · rs199832508

See detailed info → Standard

Height (baseline)

LTBP2 · rs199709938

See detailed info → Standard

Height (baseline)

CAMTA1 · rs192484863

See detailed info → Standard

Height (baseline)

near LINC02571 · rs191989932

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Height

near Metazoa_SRP · rs1911223

See detailed info → Standard

Height (baseline)

CRADD · rs188516017

See detailed info → Standard

Height (baseline)

LIN28B · rs188162353

See detailed info → Standard

Height (baseline)

PDE6D · rs187368135

See detailed info → Standard

Height

ZNF252P-AS1 · rs187149998

See detailed info → Standard

Height

near H4C11 · rs182819650

See detailed info → Standard

Height

near HNRNPKP3 · rs17580259

See detailed info → Standard

Height

ZNF516 · rs17059354

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Showing 20 of 11486 · page 273 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.