Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,083 positions on this site are linked to Height, out of 2,506,337 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)

LIN28B · rs62419605

See detailed info → Standard

Height (baseline)

MFGE8 · rs28384224

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Height

ADAR · rs2335230

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Height

CRHR1 · rs17689882

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Height

NCOA2 · rs16936922

See detailed info → Standard

Height

GLI3 · rs11983409

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Height

near CBX7 · rs738469

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Height (standard GWA)

DRAIC · rs35281701

See detailed info → Standard

Height

LIN28B-AS1 · rs12207399

See detailed info → Standard

Height

PARPBP · rs76157805

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Height (baseline)

ACAN · rs4932435

See detailed info → Standard

Height (baseline)

EPB41L1-AS1 · rs142636887

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Height

CACNA1H · rs4984636

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Height

GAS7 · rs2157696

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Height (baseline)

near RPF2P1 · rs118102692

See detailed info → Standard

Height

near RNF26 · rs2511847

See detailed info → Standard

Height (baseline)

LINC02996 · rs62370525

See detailed info → Standard

Height (baseline)

WNT9A · rs79735944

See detailed info → Standard

Height (baseline)

ITCH · rs143965658

See detailed info → Standard

Height (baseline)

ADCY3 · rs11678026

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Showing 20 of 11083 · page 184 of 555

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.