Gene Knowledge Graph

UTC

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

11,696 positions on this site are linked to Height, out of 2,512,461 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

Height (baseline)

NBEAL2 · rs529229466

See detailed info → Standard

Height (baseline)

ECE1 · rs213022

See detailed info → Standard

Height

near UBE2V1 · rs1000595

See detailed info → Standard

Height

SLC41A2 · rs7299019

See detailed info → Standard

Height (baseline)

SLC9A4 · rs2310303

See detailed info → Standard

Height

near CABLES1 · rs8096254

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Height (baseline)

near STAU1 · rs74744146

See detailed info → Standard

Height (baseline)

NFIC · rs56230484

See detailed info → Standard

Height

ZNF638 · rs12612930

See detailed info → Standard

Standing height (UKB data field 50)

PITX1-AS1 · rs9327705

See detailed info → Standard

Height (baseline)

near INSYN1-AS1 · rs874956

See detailed info → Standard

Height (baseline)

near SDR16C6P · rs62516734

See detailed info → Standard

Height

SYMPK · rs3745929

See detailed info → Standard

Height

near NPM1P47 · rs17271431

See detailed info → Standard

Height (baseline)

IGF1R · rs149779029

See detailed info → Standard

Height (baseline)

IARS1 · rs78155973

See detailed info → Standard

Height

near MIR17HG · rs7327945

See detailed info → Standard

Height (baseline)

MARS1 · rs7304550

See detailed info → Standard

Height

near RNU2-36P · rs171340

See detailed info → Standard

Height (baseline)

RFC1 · rs12501447

See detailed info →

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.