Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,464 positions on this site are linked to Height, out of 2,509,249 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

TIAM1 · rs13050704

See detailed info → Standard

Height (baseline)

DYSF · rs13028056

See detailed info → Standard

Height (baseline)

near SMIM23 · rs12651846

See detailed info → Standard

Height

RPGRIP1L · rs12598253

See detailed info → Standard

Height

MAPK1IP1L · rs12589920

See detailed info → Standard

Height

DOCK5 · rs12542851

See detailed info → Standard

Height

near LINC02533 · rs12206941

See detailed info → Standard

Height (baseline)

GLCCI1 · rs12155035

See detailed info → Standard

Height (baseline)

near HNRNPA1P67 · rs11947772

See detailed info → Standard

Height (baseline)

near IFNGR2 · rs11908875

See detailed info → Standard

Height (baseline)

near PRKCA · rs11867898

See detailed info → Standard

Height (baseline)

near CD276 · rs118083619

See detailed info → Standard

Height

KIF13B · rs11786952

See detailed info → Standard

Height (baseline)

ZNF652 · rs117328129

See detailed info → Standard

Height (baseline)

near CLNK · rs11721691

See detailed info → Standard

Height

SATB1 · rs11716005

See detailed info → Standard

Height (baseline)

near IGF2 · rs116869930

See detailed info → Standard

Height

POLR2A · rs116560331

See detailed info → Standard

Height

near Y_RNA · rs11622421

See detailed info → Standard

Height (baseline)

LYPLAL1-AS1 · rs115945763

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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.