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 10, 2026

11,479 positions on this site are linked to Height, out of 2,509,486 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 (standard GWA)

near ZNF619P1 · rs10252568

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Standard

Height

near ZMAT4 · rs1022192

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Standard

Height

LARGE1 · rs1018786

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Standard

Height

SRMP3 · rs10184951

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Standard

Height

SLF1 · rs10041551

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Standard

Height

ADAMTS3 · rs10027494

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Standard

Height

TEKT5 · rs9932893

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Standard

Height

CRELD2 · rs9616380

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Standard

Height (standard GWA)

near STOML3 · rs9576685

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Standard

Height

ARHGEF7 · rs9515399

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Standard

Height (baseline)

MKRN6P · rs9470026

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Standard

Height

QKI · rs9458846

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Standard

Height

near LINC01615 · rs9346605

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Standard

Height

DOK2 · rs899428

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Standard

Height (baseline)

near CLXN · rs878995

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Standard

Height

SUSD4 · rs851140

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Standard

Height

DAGLB · rs836510

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Standard

Height (baseline)

near RNU7-134P · rs8073169

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Standard

Height (baseline)

DHRS4-AS1 · rs8017358

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Standard

Height (baseline)

FRS2 · rs79678493

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Showing 20 of 11479 · page 267 of 574

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.