Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,048 positions on this site are linked to Height, out of 2,506,059 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

ARSB · rs16875913

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Standard

Height

near LINC02120 · rs1508821

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Height

near MRPL42 · rs12823898

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Height

LTBP4 · rs3815913

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Height

RAD18 · rs11719775

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Height

WWTR1 · rs13325622

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Height

SH2D4A · rs7814466

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Height

DIRC3 · rs6435985

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Height

LINC02166 · rs3751700

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Height

near FBLN5 · rs2498828

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Height

LMAN2L · rs56351161

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Height

near LYZL1 · rs501298

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Height

near CLEC14A · rs1168462

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Height

PACSIN2 · rs1076118

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Height

SYNE3 · rs17092197

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Height

near GHSR · rs13085429

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Height

near PWWP2A · rs11952950

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Height

near SEPHS1P2 · rs7173904

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Height

CASC20 · rs6054304

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Height

near MRPL50P4 · rs4341489

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Showing 20 of 11048 · page 169 of 553

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.