Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,645 positions on this site are linked to Height, out of 2,511,617 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)

DIS3L2 · rs149870557

See detailed info → Standard

Height

near RN7SL824P · rs12132293

See detailed info → Standard

Height

near HRCT1 · rs12003547

See detailed info → Standard

Height

near CDC42EP3-AS1 · rs10173794

See detailed info → Standard

Height

DLG5 · rs1659390

See detailed info → Standard

height (mean, inv-normal transformed)

DNM3 · rs61807788

See detailed info → Standard

Height

near RNU6-13P · rs17785796

See detailed info → Standard

Height (maximum, inv-normal transformed)

DNM3 · rs11584955

See detailed info → Standard

Height

near DDX27 · rs73611371

See detailed info → Standard

Height

CRIM1 · rs3770817

See detailed info → Standard

Height

GRM4 · rs2499724

See detailed info → Standard

Height

USP8 · rs12050594

See detailed info → Standard

Height

near PCBP2P1 · rs2037923

See detailed info → Standard

Height

TICRR · rs8038028

See detailed info → Standard

Height

HDAC3 · rs2530223

See detailed info → Standard

Height

ZNF414 · rs2287863

See detailed info → Standard

Height

LINC01478 · rs2198853

See detailed info → Standard

Height

LINC01937 · rs11693678

See detailed info → Standard

Height

FMN2 · rs10926168

See detailed info → Standard

Height

PTPN14 · rs6540846

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Showing 20 of 11645 · page 28 of 583

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.