Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,206 positions on this site are linked to Height, out of 2,507,144 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 (maximum, inv-normal transformed)

SPAAR · rs2890718

See detailed info → Standard

Height

DVL2 · rs222836

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Height (baseline)

QRICH1 · rs199507730

See detailed info → Standard

Height (baseline)

LINC01755 · rs1514134

See detailed info → Standard

Height (baseline)

SPRYD3 · rs150819866

See detailed info → Standard

Height (baseline)

BPIFB5P · rs143502992

See detailed info → Standard

Height (baseline)

L3MBTL3 · rs13208867

See detailed info → Standard

Standing height (UKB data field 50)

BCAS3 · rs113347646

See detailed info → Standard

Height (baseline)

EFEMP1 · rs112149687

See detailed info → Standard

Height

near TEAD1 · rs10831889

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Height (baseline)

HLA-DQA1 · rs79034180

See detailed info → Standard

Standing height (UKB data field 50)

near ID4 · rs6936363

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Height

NICN1 · rs6446272

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Height

WDR72 · rs4143622

See detailed info → Standard

Height

near LMNB1 · rs2973593

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Height (baseline)

near UBE2V2 · rs149847310

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Height

near RNU6ATAC19P · rs11904490

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Height (baseline)

near CCT4P1 · rs73165497

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Height (baseline)

near BLM · rs404623

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Height (baseline)

TMEM259 · rs117246624

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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.