Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,865 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)

KIF9 · rs116252905

See detailed info → Standard

Height (baseline)

near LINC02547 · rs11605159

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Height (standard GWA)

TOMM20 · rs11582001

See detailed info → Standard

Height (baseline)

FAM184B · rs115398829

See detailed info → Standard

Height (baseline)

NELFE · rs114969413

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Height (baseline)

near CMPK1P1 · rs114466461

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Height (baseline)

GBF1 · rs113676575

See detailed info → Standard

Height (baseline)

PPP1R13B · rs113419453

See detailed info → Standard

Height

SLCO2B1 · rs11236368

See detailed info → Standard

Height (baseline)

near TRIM51CP · rs111648199

See detailed info → Standard

Height (baseline)

near COX7A2 · rs111637909

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Height

SLC25A38 · rs11129823

See detailed info → Standard

Height (baseline)

CLUH · rs111246591

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Height

near HLX · rs11118636

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Height (baseline)

near NACAP8 · rs11106863

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Height (baseline)

PIP4K2A · rs11013071

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Height

NFIB · rs10961429

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Height

PAPPA2 · rs10913204

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Height

TPO · rs10519477

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Height

RPS6KA2 · rs1040446

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Showing 20 of 11879 · page 354 of 594

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.