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

Height

SLC12A2-DT · rs17607234

See detailed info → Standard

Height

near NMBR · rs12212141

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Height

DLEU1 · rs475883

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Height

near ZNF619P1 · rs13239088

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Height

LCORL · rs16895917

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Height

DOC2A · rs11649274

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Height

PAPPA2 · rs2294494

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Height

DSE · rs6908915

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Height

near AP4E1 · rs2619691

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Height

SCAP · rs17784714

See detailed info → Standard

Height

MIR4744 · rs12456845

See detailed info → Standard

Height

MSRB3 · rs6581626

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Height

LPAR1 · rs10817133

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Height

near RN7SL7P · rs13240305

See detailed info → Standard

Height

ADAM7-AS1 · rs17051757

See detailed info → Standard

Height

FER · rs2113001

See detailed info → Standard

Height

UHRF1 · rs3786941

See detailed info → Standard

Height

KIZ · rs6082351

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Height

near C17orf67 · rs227705

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Height

GNA12 · rs798487

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Showing 20 of 11707 · page 61 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.