Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

10,966 positions on this site are linked to Height, out of 2,505,721 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

LRRC37B · rs17780086

See detailed info → Standard

Height

SLC38A9 · rs11958779

See detailed info → Standard

Height

C9orf64 · rs7853377

See detailed info → Standard

Height

NCKAP5 · rs7567288

See detailed info → Standard

Height

PDIA4 · rs822552

See detailed info → Standard

Height

SEPT2 · rs12694997

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Height

DYM · rs1787200

See detailed info → Standard

Height

ARSE · rs12393627

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Height

near CSH1 · rs2854160

See detailed info → Standard

Height

MAP3K3 · rs11658329

See detailed info → Standard

Height

PPARD · rs9470004

See detailed info → Standard

Height

ACAN · rs2351491

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Height

HHIP · rs1492820

See detailed info → Standard

Height

GPR126 · rs4896582

See detailed info → Standard

Height

ZRANB3 · rs1900741

See detailed info → Standard

Height

RFC1 · rs2066789

See detailed info → Standard

Height

NEPRO-AS1 · rs1903431

See detailed info → Standard

Height

TMEM229B · rs8019974

See detailed info → Standard

Height

GNA12 · rs2266925

See detailed info → Standard

Height

FOXP4 · rs912883

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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.