Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,960 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)

near MOS · rs142856921

See detailed info → Standard

Height

LINC01182 · rs1426126

See detailed info → Standard

Height (baseline)

near SOCS2 · rs142519563

See detailed info → Standard

Height (baseline)

near CD3E · rs141752759

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs139578288

See detailed info → Standard

Height (baseline)

near TMED7 · rs139443511

See detailed info → Standard

Height

near Y_RNA · rs1389325

See detailed info → Standard

Height (baseline)

near RN7SL316P · rs138044297

See detailed info → Standard

Height (baseline)

near HCAR1 · rs137929115

See detailed info → Standard

Height

PTPRK · rs1341597

See detailed info → Standard

Height

DIS3L2 · rs13412942

See detailed info → Standard

Height (baseline)

CSNK1G3 · rs13190325

See detailed info → Standard

Height

OSBPL10 · rs13070370

See detailed info → Standard

Height

DSEL-AS1 · rs12967353

See detailed info → Standard

Height

RARB · rs1286654

See detailed info → Standard

Height

MYO6 · rs1280052

See detailed info → Standard

Height (baseline)

PIK3R1 · rs12652661

See detailed info → Standard

Height

IGF2BP2-AS1 · rs12635769

See detailed info → Standard

Height

CDK14 · rs12537076

See detailed info → Standard

Height (standard GWA)

AFG1L · rs12526579

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Showing 20 of 11879 · page 352 of 594

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.