Gene Knowledge Graph
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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

11,493 positions on this site are linked to Height, out of 2,509,702 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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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 ATP5F1AP2 · rs11683995

See detailed info → Standard

Height

EML5 · rs11628848

See detailed info → Standard

Height (baseline)

FNDC3B · rs116145037

See detailed info → Standard

Height

EPC1-AS1 · rs11592205

See detailed info → Standard

Height (baseline)

EDEM3 · rs115585866

See detailed info → Standard

Height (baseline)

DNM3 · rs114860572

See detailed info → Standard

Height (baseline)

near ABT1 · rs114462827

See detailed info → Standard

Height (baseline)

near KRT18P51 · rs114391511

See detailed info → Standard

Height (baseline)

near ZNF346 · rs113056884

See detailed info → Standard

Height

SFMBT2 · rs11255111

See detailed info → Standard

Height

GRM1 · rs10872583

See detailed info → Standard

Height (baseline)

LINC01755 · rs10789012

See detailed info → Standard

Height

near TRPC6P9 · rs10473657

See detailed info → Standard

Height

PDE5A · rs1045177

See detailed info → Standard

Height

MYO9B · rs10423232

See detailed info → Standard

Height

DNAJB12 · rs10400019

See detailed info → Standard

Height

DGKG · rs9877630

See detailed info → Standard

Height

LINC01478 · rs9807203

See detailed info → Standard

Height (baseline)

near POLR2A · rs9630723

See detailed info → Standard

Height

near LINC00343 · rs9519836

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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.