Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 11, 2026

11,639 positions on this site are linked to Height, out of 2,511,480 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

HDAC9 · rs2526640

See detailed info → Standard

Height

SMIM29-AS1 · rs9366846

See detailed info → Standard

Height

EFR3B · rs6734859

See detailed info → Standard

Height

MIRLET7A1HG · rs10821311

See detailed info → Standard

Height

LTBP2 · rs3825710

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Height

SLCO1C1 · rs10770705

See detailed info → Standard

Height

near U2 · rs12005413

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Height

KCNJ12 · rs1317349

See detailed info → Standard

Height

ZCCHC8 · rs10773208

See detailed info → Standard

Height

near ZNF878 · rs7254539

See detailed info → Standard

Height

HDLBP · rs1134941

See detailed info → Standard

Height

LTBP1 · rs41464348

See detailed info → Standard

Height

EPB41L2 · rs6921207

See detailed info → Standard

Height

PNKD · rs992157

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Height

near ANKRD9 · rs8011721

See detailed info → Standard

Height

LOXL2 · rs4278162

See detailed info → Standard

Height

near RBBP8 · rs10853489

See detailed info → Standard

Height

near SERBP1P3 · rs2564926

See detailed info → Standard

Height

MIR17HG · rs7320982

See detailed info → Standard

Height

near LINC02995 · rs7704555

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Showing 20 of 11639 · page 17 of 582

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.