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 2,506,432 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)

SLC13A4 · rs111545354

See detailed info → Standard

Height

MAPKAPK2 · rs10863784

See detailed info → Standard

Height

near LINC02667 · rs10829518

See detailed info → Standard

Height

SH3GL3 · rs10520579

See detailed info → Standard

Height

EPCAM-DT · rs10514804

See detailed info → Standard

Height

near LINC02852 · rs1035649

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Height

FRMD6 · rs10141001

See detailed info → Standard

Height

USP4 · rs9874474

See detailed info → Standard

Height

EHMT2 · rs9501159

See detailed info → Standard

Height (baseline)

near GLIS2 · rs804176

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Height

ABHD17C · rs8025914

See detailed info → Standard

Height

CHTOP · rs7549308

See detailed info → Standard

Height (baseline)

LTBP1 · rs75263017

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

FAM149B1 · rs74423725

See detailed info → Standard

Height

VEPH1 · rs73156789

See detailed info → Standard

Height

MSRB3 · rs7306826

See detailed info → Standard

Standing height (UKB data field 50)

near ARID1B · rs73013270

See detailed info → Standard

Height (baseline)

near OXCT1 · rs72761807

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Height

near NTRK2 · rs726432

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Height

near ABCC10 · rs6907066

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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.