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 10, 2026

11,616 positions on this site are linked to Height, out of 2,511,293 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 (baseline)

HLA-DRB5 · rs541542451

See detailed info → Standard

Height (baseline)

FBP2 · rs2460137

See detailed info → Standard

Height (baseline)

ATF6B · rs144354976

See detailed info → Standard

Height (baseline)

DNM3 · rs9425601

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Height

CPA3 · rs4681161

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Height (baseline)

PIEZO1 · rs2278053

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Height (baseline)

DLEU1 · rs147009283

See detailed info → Standard

Height

NCAPD3 · rs73731

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Height

near Y_RNA · rs6892539

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Height

NPR3 · rs976576

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Height

PDE10A · rs893310

See detailed info → Standard

Height (baseline)

NBEAL2 · rs529229466

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Height (baseline)

ECE1 · rs213022

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Height

near UBE2V1 · rs1000595

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Height

SLC41A2 · rs7299019

See detailed info → Standard

Height (baseline)

SLC9A4 · rs2310303

See detailed info → Standard

Height

near CABLES1 · rs8096254

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Height (baseline)

near STAU1 · rs74744146

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Height (baseline)

NFIC · rs56230484

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Height

ZNF638 · rs12612930

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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.