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

11,272 positions on this site are linked to Height, out of 2,507,630 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

LINC01936 · rs183514801

See detailed info → Standard

Height (baseline)

near H3P24 · rs1833628

See detailed info → Standard

Height

NUDT4 · rs17837158

See detailed info → Standard

Height

near WWTR1 · rs17787916

See detailed info → Standard

Height

near RASGRP4 · rs17640544

See detailed info → Standard

Height (standard GWA)

HDAC9 · rs1726599

See detailed info → Standard

Height

FAM227B · rs16962663

See detailed info → Standard

Height

near LINC02181 · rs16942624

See detailed info → Standard

Height

MAPK14 · rs16884650

See detailed info → Standard

Height

DELEC1 · rs1556220

See detailed info → Standard

Height (baseline)

near ZNF592 · rs149291365

See detailed info → Standard

Height (baseline)

near LINC01365 · rs141656367

See detailed info → Standard

Height (baseline)

near BARX1 · rs140868036

See detailed info → Standard

Height

SCML2 · rs137959675

See detailed info → Standard

Height (baseline)

near SERPINE1 · rs13238709

See detailed info → Standard

Height (baseline)

PDE4D-AS1 · rs13181587

See detailed info → Standard

Height (baseline)

PML · rs12911485

See detailed info → Standard

Height (baseline)

B4GALNT3 · rs12821124

See detailed info → Standard

Height (standard GWA)

CACUL1 · rs12774262

See detailed info → Standard

Height (baseline)

DDAH1 · rs12726532

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.