Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,146 positions on this site are linked to Height, out of 2,506,622 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

PAH · rs7964033

See detailed info → Standard

Height (baseline)

near HSPA8P5 · rs78976491

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Height (baseline)

ATP5MC2 · rs78884307

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Height (baseline)

near OR9G3P · rs77759547

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Height

near NUP50P4 · rs7752646

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height (minimum, inv-normal transformed)

BMP2K · rs7660310

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Height

SUCLG2 · rs7620956

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Height (baseline)

OTUD7B · rs751931

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Height (baseline)

WWP2 · rs75109048

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Height

ARID2 · rs7310939

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Height

ATF7IP · rs7308681

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Height (baseline)

TMEM244 · rs72993254

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Height (baseline)

near BAZ2B-AS1 · rs72956103

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Height

P3H2 · rs710550

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Height

PCSK5 · rs7031971

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Height

JPH1 · rs6988935

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Height

near TMEM272 · rs686321

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Standing height (UKB data field 50)

FAM114A1 · rs6820957

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What is your height? (cm, inv-normal transformed)

near CYTH1 · rs6501238

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Height (baseline)

LIN28B-AS1 · rs62419583

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Showing 20 of 11146 · page 380 of 558

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.