Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,515 positions on this site are linked to Height, out of 2,509,918 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 PPFIA2 · rs139770682

See detailed info → Standard

Height

CTD-2023 N9.1 · rs554379257

See detailed info → Standard

Height

DAP · rs755546258

See detailed info → Standard

Height

NPR3 · rs72742734

See detailed info → Standard

Height

near PPP1R3A · rs184469050

See detailed info → Standard

Height

CMTM8 · rs6765866

See detailed info → Standard

Height

RP11-317P15.6 · rs558671668

See detailed info → Standard

Height

RP1-35C21.2 · rs146949893

See detailed info → Standard

Height

ZNF678 · rs1390401

See detailed info → Standard

Height

C6orf106 · rs2814993

See detailed info → Standard

Height

IHH · rs6724465

See detailed info → Standard

Height

GPR126 · rs3748069

See detailed info → Standard

Sitting height ratio

NFATC2 · rs228836

See detailed info → Standard

Height

EXTL3 · rs10448080

See detailed info → Standard

Height

SLC17A2 · rs1865760

See detailed info → Standard

Height

TLE3 · rs10152591

See detailed info → Standard

Height

CCDC108/IHH · rs12470505

See detailed info → Standard

Height

JMJD4 · rs10799445

See detailed info → Standard

Height

ATP5SL · rs17318596

See detailed info → Standard

Height

DIS3L2 · rs3103267

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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.