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 2,506,243 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

near RNA5SP267 · rs35484123

See detailed info → Standard

height (mean, inv-normal transformed)

DRAIC · rs34549281

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Height (baseline)

CPNE1 · rs28634878

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Height

LINC01258 · rs2637718

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Height (baseline)

near SMIM23 · rs11949845

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Height (baseline)

MAP4 · rs137940588

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Height (baseline)

near ECEL1 · rs115102757

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Height (baseline)

near TENT5A · rs112178137

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Height (baseline)

ANKS1A · rs142141811

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Height

near LIF-AS1 · rs2073946

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Height

EMC3 · rs13096737

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Height

near LINC01247 · rs12997617

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Height

PSD3 · rs6992325

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Height (baseline)

PHF21A · rs2959093

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Height (baseline)

ZSCAN16 · rs200185462

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Standing height (UKB data field 50)

KIF1B · rs7524908

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Height

ELF1 · rs7335629

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Height

MECOM · rs16853650

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Height

SMOX · rs1337281

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Standing height (UKB data field 50)

HLA-DQB2 · rs78631708

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Showing 20 of 11048 · page 181 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.