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

11,114 positions on this site are linked to Height, out of 2,506,525 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 LMAN2L · rs6746896

See detailed info → Standard

Height

near SNED1 · rs4344930

See detailed info → Standard

Height

NALCN-AS1 · rs8922

See detailed info → Standard

Height

near UPF3A · rs7998612

See detailed info → Standard

Height

CCDC80 · rs6807798

See detailed info → Standard

Height

ATP6V0D1 · rs2279023

See detailed info → Standard

Height

near ISG20 · rs6496519

See detailed info → Standard

Height

NUP37 · rs2271266

See detailed info → Standard

Height

near FBLN5 · rs2430339

See detailed info → Standard

Height (standard GWA)

near BMP6 · rs7741360

See detailed info → Standard

Height

SEMA6D · rs6493265

See detailed info → Standard

Height

PLEKHA6 · rs11240716

See detailed info → Standard

Height

KCNJ15 · rs9983358

See detailed info → Standard

Height

PLPP3 · rs1572057

See detailed info → Standard

Height

GLRX · rs10515229

See detailed info → Standard

Height (baseline)

UQCC1 · rs117968629

See detailed info → Standard

Height

PRKCE · rs7578578

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

FER · rs55954478

See detailed info → Standard

Height (baseline)

SPAG4 · rs2425067

See detailed info → Standard

Height

MICAL3 · rs2587109

See detailed info →

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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.