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 9, 2026

11,351 positions on this site are linked to Height, out of 2,508,348 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 (baseline)

NFIC · rs9748965

See detailed info → Standard

Height

TRAM2 · rs941969

See detailed info → Standard

Height (baseline)

SYNE1 · rs9397486

See detailed info → Standard

Height (baseline)

near CYB5B · rs8054363

See detailed info → Standard

Height (baseline)

TRMT1L · rs79919395

See detailed info → Standard

Height (baseline)

DUSP16 · rs79687643

See detailed info → Standard

Height (baseline)

FNIP1 · rs79577858

See detailed info → Standard

Height (baseline)

MRPL23 · rs7945810

See detailed info → Standard

Height

UBASH3B · rs7940959

See detailed info → Standard

Height

AUTS2 · rs79048874

See detailed info → Standard

Height (baseline)

FAM240A · rs79036361

See detailed info → Standard

Height (baseline)

near TRPS1 · rs78524196

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Height

TG · rs7844761

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Height (baseline)

near NACA2 · rs77893494

See detailed info → Standard

Height (baseline)

TRPS1 · rs77193180

See detailed info → Standard

Height

near AMD1P1 · rs77164188

See detailed info → Standard

Height (baseline)

FST · rs76803798

See detailed info → Standard

Height (baseline)

PDK4-AS1 · rs76276659

See detailed info → Standard

Height (baseline)

NAV3 · rs76219170

See detailed info → Standard

Height (baseline)

AGAP1 · rs7590181

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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.