Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,575 positions on this site are linked to Height, out of 2,510,695 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)

HCG27 · rs568261699

See detailed info → Standard

Height

ADAMTSL3 · rs17158445

See detailed info → Standard

Height (baseline)

PLAG1 · rs76373628

See detailed info → Standard

Height

KCNQ1 · rs163183

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Height (baseline)

FLJ40194 · rs146264265

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Height (baseline)

ADAMTS17 · rs144331869

See detailed info → Standard

Height

ANTXR1 · rs10179227

See detailed info → Standard

Height

TRIP11 · rs7154721

See detailed info → Standard

Standing height (UKB data field 50)

ZNF521 · rs6508355

See detailed info → Standard

Standing height (UKB data field 50)

LINC02895 · rs1393418

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Height (maximum, inv-normal transformed)

near ADAMTS2 · rs7722790

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Height (baseline)

PNPT1 · rs76693423

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Height (baseline)

CTPS1 · rs72663737

See detailed info → Standard

Height

SLC22A1 · rs594709

See detailed info → Standard

Height (baseline)

FANCC · rs549658720

See detailed info → Standard

Height (baseline)

LIN28A · rs35184161

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Height (baseline)

FER · rs35137434

See detailed info → Standard

Height (baseline)

PDE3A · rs76274569

See detailed info → Standard

Standing height (UKB data field 50)

PCSK5 · rs3739728

See detailed info → Standard

Height (baseline)

DDX42 · rs150030396

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Showing 20 of 11575 · page 560 of 579

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.