Gene Knowledge Graph

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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,525 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Height (baseline)

DIRC3 · rs74411434

See detailed info → Standard

Height

ADAMTS17 · rs1383543

See detailed info → Standard

Height (baseline)

ZRANB2 · rs66461782

See detailed info → Standard

Height (baseline)

LCORL · rs74537632

See detailed info → Standard

Standing height (UKB data field 50)

near NIP7P1 · rs117327710

See detailed info → Standard

Height

RND3 · rs2222760

See detailed info → Standard

Height

near PDE4B · rs11208844

See detailed info → Standard

Height

near TOM1L1 · rs2934901

See detailed info → Standard

Height (baseline)

PPP3R1 · rs75483778

See detailed info → Standard

Height

TTC28 · rs76450219

See detailed info → Standard

Height

near SLC7A6 · rs9888986

See detailed info → Standard

Height

SKOR1-AS1 · rs3803522

See detailed info → Standard

Height (baseline)

near SOCS2 · rs11107138

See detailed info → Standard

Standing height (UKB data field 50)

ZNF24TR · rs34849253

See detailed info → Standard

Height

GALNT2 · rs612577

See detailed info → Standard

Height

ESR1 · rs3020418

See detailed info → Standard

Height

ADAMTS3 · rs9993613

See detailed info → Standard

Height (baseline)

LRP5 · rs314779

See detailed info → Standard

Height

BCKDHB · rs660888

See detailed info → Standard

Height (baseline)

NUDT6 · rs12509014

See detailed info →

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.