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 11, 2026

11,645 positions on this site are linked to Height, out of 2,511,803 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

MGAT1 · rs3733750

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Standard

Height

DYM · rs2078286

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Height

CAV2-DT · rs1918917

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Height

near PKDCC · rs12479347

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Height

near RN7SL396P · rs6981251

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Height

near RNA5SP455 · rs603354

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Height

UST · rs2153252

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Height

ADAMTS17 · rs1383546

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Height

near LINC02409 · rs10860152

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Height

LNX1 · rs6855607

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Height

near RPL23AP44 · rs4385235

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Height

ZBTB20 · rs9855047

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Height

NUP153 · rs6927877

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Height

TSPO · rs6972

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Height

CADPS2 · rs17463319

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Height

near TUG1 · rs4820921

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Height

RGL1 · rs11591089

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Height

REPS1 · rs973170

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Height

ZFHX3 · rs4887925

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Height

COL6A3 · rs2645772

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Showing 20 of 11645 · page 31 of 583

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.