Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,083 positions on this site are linked to Height, out of 2,506,337 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

near RNA5SP326 · rs1676783

See detailed info → Standard

Height (baseline)

LRCH1 · rs1570622

See detailed info → Standard

Height (baseline)

PLCD4 · rs147343205

See detailed info → Standard

Height (baseline)

GUSBP5 · rs147277890

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Height

near HSP90AB3P · rs1463099

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Height

ZNF471 · rs13346710

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Height

near KRT18P3 · rs13037670

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Height

near GNA13 · rs12939956

See detailed info → Standard

Height

near PHACTR2 · rs12663714

See detailed info → Standard

Standing height (UKB data field 50)

SLC30A10 · rs12096993

See detailed info → Standard

Height

near SPACA1 · rs11968732

See detailed info → Standard

Height

MATN1 · rs1188394

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Height (baseline)

near RNA5SP362 · rs11832742

See detailed info → Standard

Height

GNA12 · rs1182176

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Height

near LINC02817 · rs11802047

See detailed info → Standard

Height (baseline)

near RNU6-1 · rs117535362

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Height

near CTDSPL · rs11711286

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Height (baseline)

AP4E1 · rs116901461

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Height (baseline)

near LINC02750 · rs11525480

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Height (baseline)

near CKAP4 · rs1148415

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Showing 20 of 11083 · page 389 of 555

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.