Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 15, 2026

5,436 positions on this site are linked to Height, out of 2,525,493 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

CPAMD8 · rs17196155

See detailed info → Standard

Height

HTD2 · rs14927

See detailed info → Standard

Height

TBX15 · rs12742627

See detailed info → Standard

Height (baseline)

DLEU1 · rs7997464

See detailed info → Standard

Height

CCDC26 · rs7814618

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Height

near RN7SL66P · rs7597744

See detailed info → Standard

Height

GRM4 · rs3887555

See detailed info → Standard

Height

PTPRG · rs1320232

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Height

near POLR1F · rs12700054

See detailed info → Standard

Height

TEAD1 · rs10831915

See detailed info → Standard

Height

near U6 · rs8014112

See detailed info → Standard

Height

LINC00184 · rs3850718

See detailed info → Standard

Height

COL27A1 · rs1982850

See detailed info → Standard

Height

SIRT6 · rs350844

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Height

near CYP2AB1P · rs2176827

See detailed info → Standard

Height

SLC22A17 · rs12896494

See detailed info → Standard

Height

near WNT5A · rs557077

See detailed info → Standard

Height

DLC1 · rs11776451

See detailed info → Standard

Height

near LINC01354 · rs271764

See detailed info → Standard

Height

near NFYCP2 · rs13290575

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Showing 20 of 5436 · page 4 of 272

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.