Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,575 positions on this site are linked to Height, out of 2,510,695 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)

CRLF3 · rs141870697

See detailed info → Standard

Height (baseline)

ATP6V1E2 · rs13008445

See detailed info → Standard

Height (baseline)

ZNF892 · rs113996403

See detailed info → Standard

Height (maximum, inv-normal transformed)

near AVPR1A · rs11174852

See detailed info → Standard

Height

ZNF143 · rs10770035

See detailed info → Standard

Height (baseline)

HMGA2 · rs73121706

See detailed info → Standard

Height (baseline)

CBFA2T2 · rs73119111

See detailed info → Standard

Height (baseline)

near HLA-DQA1 · rs534868470

See detailed info → Standard

Height

KCNJ12 · rs4488509

See detailed info → Standard

Height (baseline)

SAPCD1-AS1 · rs28399993

See detailed info → Standard

Height

SMIM29-AS1 · rs148899910

See detailed info → Standard

Height (baseline)

FUBP3 · rs11789553

See detailed info → Standard

Height (baseline)

CRADD-AS1 · rs111599540

See detailed info → Standard

Height

near EPS15P1 · rs1464841

See detailed info → Standard

Height

ISM1 · rs719628

See detailed info → Standard

Height

ADGRL3 · rs573890687

See detailed info → Standard

Height (baseline)

NSF · rs117300236

See detailed info → Standard

Height

PSMC3 · rs10838708

See detailed info → Standard

Height

SLC4A4 · rs1840086

See detailed info → Standard

Height

VAMP9P · rs6822283

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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.