Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,707 positions on this site are linked to Height, out of 2,512,507 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

Standing height (UKB data field 50)

ESR2 · rs2772163

See detailed info → Standard

Standing height (UKB data field 50)

near MFSD14B · rs192122412

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Height (baseline)

near HHIP-AS1 · rs140425465

See detailed info → Standard

Height

near NCLN · rs12460720

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Height

near LINC02667 · rs11598539

See detailed info → Standard

Height (baseline)

near BMP6 · rs11243201

See detailed info → Standard

Height (baseline)

near MANBAL · rs6017776

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height (mean, inv-normal transformed)

METAP2 · rs301033

See detailed info → Standard

Height (baseline)

AMZ1 · rs2266920

See detailed info → Standard

Standing height (UKB data field 50)

BMP6 · rs17605530

See detailed info → Standard

Height

POSTN · rs17197663

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Height (baseline)

LIPG · rs8096042

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Height (baseline)

near UQCC1 · rs76660268

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Height

FANCI · rs7168941

See detailed info → Standard

Height (baseline)

TBX2-AS1 · rs138987744

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Height (baseline)

near POMC · rs34914018

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Height (baseline)

TSC2 · rs17654678

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Height

LRRC45 · rs11659000

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Height (baseline)

near UBE2Q2P8 · rs11636961

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Height

near PMP22 · rs10852830

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Showing 20 of 11707 · page 564 of 586

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.