Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 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)

LINC01505 · rs12377541

See detailed info → Standard

Height (baseline)

near MOGAT3 · rs12333363

See detailed info → Standard

Height

LCOR · rs12258355

See detailed info → Standard

Height

NCBP3 · rs1183148

See detailed info → Standard

Height

CEP164 · rs11822288

See detailed info → Standard

Height (baseline)

near CSH1 · rs118048414

See detailed info → Standard

Height

ASAP2 · rs11688860

See detailed info → Standard

Height (baseline)

LAMB2P1 · rs116285936

See detailed info → Standard

Height

near SLC35B4 · rs1158579

See detailed info → Standard

Height (baseline)

PTPRJ · rs113408284

See detailed info → Standard

Height (baseline)

FBXL2 · rs112986417

See detailed info → Standard

Height (baseline)

DENR · rs112898406

See detailed info → Standard

Height

TET1 · rs10998375

See detailed info → Standard

Height (baseline)

LHPP · rs10901772

See detailed info → Standard

Height

MIR3681HG · rs10495598

See detailed info → Standard

Height

PCSK6 · rs10152756

See detailed info → Standard

Height (baseline)

RTN1 · rs10137320

See detailed info → Standard

Height

BTBD9 · rs9296239

See detailed info → Standard

Height

near ACVR1B · rs877868

See detailed info → Standard

Height

EGFR-AS1 · rs845559

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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.