Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,525 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)

LAMB2 · rs62262519

See detailed info → Standard

Height (baseline)

PEX14 · rs60321516

See detailed info → Standard

Height (maximum, inv-normal transformed)

YWHAB · rs6031860

See detailed info → Standard

Height (baseline)

near ANAPC10 · rs572869023

See detailed info → Standard

Height (baseline)

near OPRD1 · rs569356

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Height (baseline)

RAB11FIP4 · rs56024867

See detailed info → Standard

Height (baseline)

near HLA-DQB1 · rs558693707

See detailed info → Standard

Standing height (UKB data field 50)

near SERPINH1 · rs557454131

See detailed info → Standard

Height (baseline)

SPI1 · rs544501401

See detailed info → Standard

Height (baseline)

ANKRD29 · rs528133362

See detailed info → Standard

Height

PCGF2 · rs4795311

See detailed info → Standard

Height

CRISPLD2 · rs4783092

See detailed info → Standard

Height

ZNF236 · rs470795

See detailed info → Standard

Height

ATR · rs4256152

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Height

near RN7SL668P · rs41437647

See detailed info → Standard

Height (baseline)

near EFS · rs3759609

See detailed info → Standard

Height

ZNF767P · rs3735320

See detailed info → Standard

Height

near MCUR1 · rs365178

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Height (baseline)

near MAB21L4 · rs35760630

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Height (baseline)

near TMEM102 · rs34280588

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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.