Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 positions on this site are linked to Height, out of 2,509,486 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)

COL24A1 · rs142389174

See detailed info → Standard

Height (baseline)

near NOG · rs142255801

See detailed info → Standard

Height (baseline)

GZMA · rs141832139

See detailed info → Standard

Height (baseline)

near PSMC1P2 · rs141504727

See detailed info → Standard

Height (standard GWA)

CPD · rs141167135

See detailed info → Standard

Height (baseline)

near UPF2 · rs141058852

See detailed info → Standard

Height (baseline)

near EIF4G3 · rs139563830

See detailed info → Standard

Height

near PSAT1 · rs1394935

See detailed info → Standard

Height (baseline)

near GAPDHP27 · rs138833816

See detailed info → Standard

Height (baseline)

PDZD2 · rs138289892

See detailed info → Standard

Height (baseline)

LRRC78P · rs137888475

See detailed info → Standard

Height

NXN · rs13353187

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Height

near RPS19P6 · rs13285452

See detailed info → Standard

Height (baseline)

STAU2 · rs13273010

See detailed info → Standard

Height (baseline)

CFAP418-AS1 · rs13254354

See detailed info → Standard

Height (baseline)

near KRT18P25 · rs13148906

See detailed info → Standard

Height (baseline)

FSTL1 · rs13088020

See detailed info → Standard

Height (baseline)

RARB · rs1303630

See detailed info → Standard

Height (baseline)

near MBD5 · rs12997473

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Height

near SPATA33 · rs12918773

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Showing 20 of 11486 · page 275 of 575

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.