Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,504 positions on this site are linked to Height, out of 2,509,702 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)

SPATA7 · rs146936137

See detailed info → Standard

Height (baseline)

SELENOP · rs146689548

See detailed info → Standard

Height (baseline)

CPLANE1 · rs144998614

See detailed info → Standard

Height

near RNU7-2P · rs144980344

See detailed info → Standard

Height (baseline)

COL5A2 · rs144317055

See detailed info → Standard

Height

near LINC02667 · rs144225905

See detailed info → Standard

Height (baseline)

KLHL29 · rs142886974

See detailed info → Standard

Height

near KANTR · rs142812240

See detailed info → Standard

Height

near ESM1 · rs1423253

See detailed info → Standard

Height (baseline)

DLGAP4 · rs140990938

See detailed info → Standard

Height (standard GWA)

near MCIDAS · rs140646985

See detailed info → Standard

Height

near MIR5197 · rs1363668

See detailed info → Standard

Height

ZNF536 · rs1347169

See detailed info → Standard

Height

ZNF618 · rs13297916

See detailed info → Standard

Height

EGR3-AS1 · rs13278111

See detailed info → Standard

Height (baseline)

NYAP1 · rs13235951

See detailed info → Standard

Height

CACNA2D1 · rs13235513

See detailed info → Standard

Height (baseline)

LINC02694 · rs12908794

See detailed info → Standard

Height

TRAF3 · rs12898022

See detailed info → Standard

Height

NR1I2 · rs12721615

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Showing 20 of 11504 · page 315 of 576

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.