Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,607 positions on this site are linked to Height, out of 2,511,197 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

RAB11A · rs2727102

See detailed info → Standard

Height

SLC4A1 · rs2074108

See detailed info → Standard

Height

DLEU1 · rs2049286

See detailed info → Standard

Height

LINC02384 · rs2006293

See detailed info → Standard

Height (baseline)

TGFB2-OT1 · rs17500758

See detailed info → Standard

Height (baseline)

CRADD · rs17021591

See detailed info → Standard

Height

CHD9 · rs16952119

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs141770783

See detailed info → Standard

Height

PDE1C · rs12534148

See detailed info → Standard

Height

EML1 · rs1191104

See detailed info → Standard

Height

CAB39L · rs11839149

See detailed info → Standard

Height

LINC01505 · rs11792623

See detailed info → Standard

Height

SLC2A13 · rs11174631

See detailed info → Standard

Height

LHPP · rs10901777

See detailed info → Standard

Height

ETV6 · rs1009954

See detailed info → Standard

Height

SMIM29 · rs10080749

See detailed info → Standard

Height

near JADRR · rs10034620

See detailed info → Standard

Height

LINC01673 · rs9981404

See detailed info → Standard

Height

E2F7 · rs7977749

See detailed info → Standard

Height (baseline)

NECAB3 · rs77972315

See detailed info →

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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.