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

11,639 positions on this site are linked to Height, out of 2,511,526 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

near LINC02995 · rs17738166

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Standard

height (minimum, inv-normal transformed)

near COL8A1 · rs1014514

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Standard

Height

GNAS · rs2057291

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Standing height (UKB data field 50)

RILPL2 · rs28481863

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Standard

Height

SKI · rs12743493

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Standard

Height

ZNF638 · rs3771371

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Standard

Height

LPP · rs6787621

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Standard

Height

CDK12 · rs6503521

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height (mean, inv-normal transformed)

ATAD5 · rs76947600

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Standard

Height

CASC15 · rs196051

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Standard

Height

ADGRG6 · rs1040525

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Height

near N4BP2 · rs794016

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Height

ADAMTS10 · rs7249094

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Height

LCORL · rs724577

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height (mean, inv-normal transformed)

PAPPA · rs7027103

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Standard

Height

PDE3A · rs6487088

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Standard

Height

GHR · rs17574650

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height (minimum, inv-normal transformed)

DOT1L · rs12983357

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Standard

Height

near PCSK5 · rs3814115

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Height

TPCN2 · rs1060435

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Showing 20 of 11639 · page 22 of 582

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.