Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,486 positions on this site are linked to Height, out of 2,509,513 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

CATSPER3 · rs537930

See detailed info → Standard

Height (baseline)

LINC02456 · rs533514283

See detailed info → Standard

Height (baseline)

near LNC-WAL · rs4801460

See detailed info → Standard

Height

CAMK1D · rs41355846

See detailed info → Standard

Height

SDK2 · rs3816995

See detailed info → Standard

Height

CPEB1 · rs2871011

See detailed info → Standard

Height

SFMBT2 · rs2762595

See detailed info → Standard

Height

MTDH · rs2331652

See detailed info → Standard

Height (baseline)

FBXW7 · rs202044741

See detailed info → Standard

Height

RBM20 · rs17763100

See detailed info → Standard

Height

LINC02456 · rs17032467

See detailed info → Standard

Height

near MTCO1P40 · rs16953054

See detailed info → Standard

Height

GPRIN3 · rs1560489

See detailed info → Standard

Height

NIPAL2 · rs1542289

See detailed info → Standard

Height (baseline)

ACAN · rs150449921

See detailed info → Standard

Height (baseline)

PTGFR · rs1410508

See detailed info → Standard

Height (baseline)

near SDHBP1 · rs13318547

See detailed info → Standard

Height (baseline)

BNC2 · rs12344619

See detailed info → Standard

Height (baseline)

ADAM7-AS1 · rs12156081

See detailed info → Standard

Height (baseline)

PAPPA2 · rs12137641

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Showing 20 of 11486 · page 279 of 575

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.