Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,464 positions on this site are linked to Height, out of 2,509,249 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 (standard GWA)

ADAMTS17 · rs59591128

See detailed info → Standard

Height

DIXDC1 · rs587774805

See detailed info → Standard

Height

NPR2 · rs5812

See detailed info → Standard

Height (baseline)

FAN1 · rs57426776

See detailed info → Standard

Height (baseline)

near GTF2IRD2P1 · rs573687632

See detailed info → Standard

Height (baseline)

ARFGEF2 · rs572131142

See detailed info → Standard

Height (baseline)

THADA · rs568331233

See detailed info → Standard

Height (baseline)

EZH1 · rs563777967

See detailed info → Standard

Height (baseline)

CDC14B · rs562388527

See detailed info → Standard

Height (baseline)

PDE3A · rs56186852

See detailed info → Standard

Height (standard GWA)

CYP20A1 · rs55939578

See detailed info → Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

NUDT6 · rs546560809

See detailed info → Standard

Height (baseline)

PPT2-EGFL8 · rs541875204

See detailed info → Standard

Height (baseline)

RAD51B · rs4902591

See detailed info → Standard

Height

near CCN3 · rs4871222

See detailed info → Standard

Height (baseline)

STK40 · rs4652909

See detailed info → Standard

Height

NECTIN3-AS1 · rs4610259

See detailed info → Standard

Height (baseline)

SLC2A9 · rs4547795

See detailed info → Standard

Height

WWOX · rs4375670

See detailed info → Standard

Height

NCAN · rs4353576

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Showing 20 of 11464 · page 247 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.