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

ZNF567 · rs8105266

See detailed info → Standard

Height (baseline)

TNRC18 · rs80186772

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Height

near RNY1P8 · rs8002827

See detailed info → Standard

Height (baseline)

near BNC1 · rs79722445

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Height

LRRC4C · rs7929217

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Height

ATRNL1 · rs7911480

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Height

GRAMD2B · rs7704203

See detailed info → Standard

Height (baseline)

KPNA7 · rs76888365

See detailed info → Standard

Height (baseline)

XXYLT1 · rs73206626

See detailed info → Standard

Height (baseline)

XPO4 · rs73167443

See detailed info → Standard

Height (baseline)

ADGRD1 · rs7312364

See detailed info → Standard

Height (baseline)

near RGS9 · rs72853511

See detailed info → Standard

Height (baseline)

ADCY3 · rs72792187

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Height (baseline)

near IARS1 · rs72748400

See detailed info → Standard

Height (baseline)

near RNU6-506P · rs72724774

See detailed info → Standard

Height

near GDPD5 · rs7128888

See detailed info → Standard

Height

near SLC45A4 · rs6992945

See detailed info → Standard

Height

near MRPL42P4 · rs6955374

See detailed info → Standard

Height

GLIS1 · rs67752113

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Height

LALTOP · rs6721842

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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.