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

11,464 positions on this site are linked to Height, out of 2,509,343 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 TNFRSF9 · rs11580517

See detailed info → Standard

Height (baseline)

CTCF · rs113775720

See detailed info → Standard

Height (baseline)

near TBX15 · rs113594268

See detailed info → Standard

Height

TSKU · rs11236938

See detailed info → Standard

Height (baseline)

near ADAR · rs112095222

See detailed info → Standard

Height

PLEC · rs11136342

See detailed info → Standard

Height

CCDC12 · rs11130111

See detailed info → Standard

Height

near LPGAT1-AS1 · rs11119820

See detailed info → Standard

Height

near OR10A5 · rs11041042

See detailed info → Standard

Height (baseline)

ZNF510 · rs10978926

See detailed info → Standard

Height

FMN2 · rs10926089

See detailed info → Standard

Height

near HTATIP2 · rs10766646

See detailed info → Standard

Height

LGR5 · rs10506632

See detailed info → Standard

Height

LRRK2 · rs10506148

See detailed info → Standard

Height (standard GWA)

near KERA · rs10492231

See detailed info → Standard

Height

near GHRHR · rs10280233

See detailed info → Standard

Height (standard GWA)

near PARTICL · rs10190585

See detailed info → Standard

Height

near OSBPL3 · rs1016916

See detailed info → Standard

Height (standard GWA)

MAPKAP1 · rs10121005

See detailed info → Standard

Height

MYLIP · rs1011616

See detailed info →

Showing 20 of 11464 · page 253 of 574

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.