Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,468 positions on this site are linked to Height, out of 2,509,343 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

LINC02030 · rs7614002

See detailed info → Standard

Height (baseline)

LINC02542 · rs76080730

See detailed info → Standard

Height (baseline)

ADAMTS6 · rs76036017

See detailed info → Standard

Height (baseline)

TSEN15 · rs75943451

See detailed info → Standard

Height (baseline)

ARID2 · rs75896254

See detailed info → Standard

Height (baseline)

GMDS · rs75455586

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Height

near RPL21P24 · rs7523969

See detailed info → Standard

Height

SBNO2 · rs74839330

See detailed info → Standard

Height (baseline)

MTUS1-DT · rs74820832

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Height

ALK · rs747148

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Height (baseline)

near SLC30A10 · rs74572621

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Height (standard GWA)

near ITM2B · rs7337883

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Height (baseline)

EPB41L1 · rs73289638

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Height

near LMNTD1 · rs7314348

See detailed info → Standard

Height (baseline)

ERC1 · rs73028374

See detailed info → Standard

Height (baseline)

SMARCA4 · rs73013166

See detailed info → Standard

Height (baseline)

DIS3L2 · rs72985631

See detailed info → Standard

Height (standard GWA)

near PRTFDC1 · rs72780323

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Height (baseline)

PIK3R1 · rs72757692

See detailed info → Standard

Height (baseline)

near FRMD3 · rs72746831

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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.