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 8, 2026

11,083 positions on this site are linked to Height, out of 2,506,432 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)

near KRT18P9 · rs62398145

See detailed info → Standard

Height (baseline)

OTUD4 · rs36227682

See detailed info → Standard

Height

near GSE1 · rs4589542

See detailed info → Standard

Height (baseline)

ECE1 · rs212515

See detailed info → Standard

Standing height (UKB data field 50)

SCMH1 · rs114198068

See detailed info → Standard

Height

GRK3-AS1 · rs5761116

See detailed info → Standard

Height

TNS2 · rs2293062

See detailed info → Standard

Height

near DIO3OS · rs10147579

See detailed info → Standard

Height (baseline)

ADAMTS17 · rs4482264

See detailed info → Standard

Height

PDE11A · rs17401468

See detailed info → Standard

Height

LNX1 · rs6820391

See detailed info → Standard

Height

near LINC02225 · rs1835874

See detailed info → Standard

Height (baseline)

PNKD · rs12993339

See detailed info → Standard

Height (baseline)

LYN · rs62515386

See detailed info → Standard

Height

GALR1 · rs58980065

See detailed info → Standard

Height

RIC3 · rs4758295

See detailed info → Standard

Height (baseline)

near PNPT1 · rs1579494

See detailed info → Standard

Height (baseline)

near RPS10P13 · rs572697180

See detailed info → Standard

Height (baseline)

near RETREG2 · rs74187143

See detailed info → Standard

Height

CFAP299 · rs6816536

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Showing 20 of 11083 · page 188 of 555

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.