Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,048 positions on this site are linked to Height, out of 2,506,152 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

NFIC · rs740521

See detailed info → Standard

Height

PELO-AS1 · rs351930

See detailed info → Standard

Standing height (UKB data field 50)

near RNU4-34P · rs149777351

See detailed info → Standard

Standing height (UKB data field 50)

PCGF5 · rs10881893

See detailed info → Standard

Height

VTI1A · rs4439449

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Height (baseline)

LIN28B-AS1 · rs118073325

See detailed info → Standard

Height (baseline)

ADAMTS17 · rs80342915

See detailed info → Standard

Height (baseline)

near LINC02160 · rs180972399

See detailed info → Standard

Height (baseline)

DOT1L · rs10669421

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Height

CHD8 · rs78484822

See detailed info → Standard

Height (baseline)

near CSH1 · rs2727346

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Height (baseline)

CDC42SE2 · rs80311787

See detailed info → Standard

Height (baseline)

near DYNLRB1 · rs565264627

See detailed info → Standard

Height (baseline)

TMBIM7P · rs79279387

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs76380397

See detailed info → Standard

Height

DNTTIP1 · rs6514062

See detailed info → Standard

Height (baseline)

near DNAJC27 · rs536780836

See detailed info → Standard

Height

IGF2R · rs9365128

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Height

EPB41L2 · rs6903066

See detailed info → Standard

Height (baseline)

NSD1 · rs371761764

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Showing 20 of 11048 · page 180 of 553

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.