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

11,159 positions on this site are linked to Height, out of 2,506,722 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

KIZ · rs2252720

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Standard

Height

ARID5B · rs4245597

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Standard

Height

near LINC02058 · rs34509

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Standard

height (mean, inv-normal transformed)

CREBRF · rs3095844

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Standard

height (minimum, inv-normal transformed)

NFIC · rs55805295

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Standard

Height

EPAS1 · rs4953353

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Standard

Height

near GRP · rs7230581

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Standard

Height

EHD3 · rs649729

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Standard

Height

COLGALT2 · rs114661926

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Standard

Height

HES7 · rs8067165

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Standard

Height

H1-10-AS1 · rs4073154

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Standard

Height

CLEC4M · rs874492

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Standard

Height

DLX6-AS1 · rs56363908

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Standard

Height

GPC5 · rs7319045

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Standard

Height

near DCUN1D4 · rs2102278

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Standard

Height

MORC3 · rs113382956

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Standard

height (mean, inv-normal transformed)

BRD3 · rs2520099

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Standard

Height

REEP5 · rs153560

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Standard

Height

DCST1 · rs74520550

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Standard

Height

LTBP1 · rs6714546

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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.