Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,159 positions on this site are linked to Height, out of 2,506,722 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

FMN1 · rs17235533

See detailed info → Standard

Height

LINC01320 · rs1718718

See detailed info → Standard

Height

AKAP12 · rs17080959

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Height (baseline)

near CXCR1 · rs16858744

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Height

near LINC02400 · rs1546189

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Height

SH3GL3 · rs1491579

See detailed info → Standard

Height (baseline)

AGPS · rs148887741

See detailed info → Standard

Height (baseline)

near HLA-DMB · rs1465651

See detailed info → Standard

Height

ADAM23 · rs1448905

See detailed info → Standard

Height

PTPRD · rs1434254

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Height

KIF13B · rs141238558

See detailed info → Standard

Standing height (UKB data field 50)

near MFGE8 · rs139811718

See detailed info → Standard

Height

near DIPK2A · rs1354496

See detailed info → Standard

Height (baseline)

CICP11 · rs13227963

See detailed info → Standard

Height

near PDLIM1 · rs12778481

See detailed info → Standard

height (mean, inv-normal transformed)

near SPRY4 · rs12658011

See detailed info → Standard

Height

GDA · rs12552331

See detailed info → Standard

Height

DLC1 · rs12547480

See detailed info → Standard

Height (baseline)

IGF2BP3 · rs12539834

See detailed info → Standard

Height

near FAM76B · rs12365735

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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.