Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,129 positions on this site are linked to Height, out of 2,506,622 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

Standing height (UKB data field 50)

ABHD15-AS1 · rs138818953

See detailed info → Standard

Standing height (UKB data field 50)

PDE4D · rs11744761

See detailed info → Standard

Height (baseline)

near IQCF2 · rs116469219

See detailed info → Standard

Height

ATF7 · rs11170624

See detailed info → Standard

Standing height (UKB data field 50)

TBX3 · rs1061651

See detailed info → Standard

Standing height (UKB data field 50)

CMAHP · rs9358839

See detailed info → Standard

Height (baseline)

DYM · rs4567803

See detailed info → Standard

Height (baseline)

PENK-AS1 · rs139744105

See detailed info → Standard

Height (baseline)

near ZNF619P1 · rs11763946

See detailed info → Standard

Height (baseline)

near HCAR1 · rs6489237

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Height

near RN7SL87P · rs2544614

See detailed info → Standard

Height (baseline)

WNT9B · rs1443311

See detailed info → Standard

Height (baseline)

SLC11A1 · rs1059823

See detailed info → Standard

Height (baseline)

BPIFB1 · rs75744141

See detailed info → Standard

Height

near MLPH · rs2325839

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Height (baseline)

KCNH6 · rs141118688

See detailed info → Standard

Height

ENDOD1 · rs7729

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Height

DIAPH1 · rs3805691

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Height (standard GWA)

GLCCI1-DT · rs37963

See detailed info → Standard

Height (baseline)

BBS9 · rs17724469

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Showing 20 of 11129 · page 530 of 557

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.