Variants linked to Height

Continuously updated · newest added Oct 25, 2026

10,261 positions on this site are linked to Height, out of 118,864 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Height

Standard

Height (baseline)

PDE3B · rs117247884

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Standard

Height (baseline)

near RN7SL554P · rs116460546

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Standard

Height (standard GWA)

near TICRR · rs11639117

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Standard

Height (standard GWA)

near RNU6-221P · rs114345761

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Standard

Height (baseline)

near LINC02747 · rs11263456

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Standard

Height (standard GWA)

near SPSB1 · rs112541935

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Standard

Height

near SYT12 · rs11227644

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Standard

Height

near LINC02784 · rs11206367

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Standard

Height

SRGAP1 · rs11175240

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Standard

Height

CALCB · rs11023392

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Standard

Height

LINC01097 · rs10939484

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Standard

Height

near PFKFB3 · rs10905876

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Standard

Height (baseline)

AK5 · rs10873946

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Standard

Height (baseline)

near SERF1AP1 · rs10857203

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Standard

Height

near MRM3P1 · rs10828243

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Standard

Height (baseline)

UPK3A · rs1057356

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Standard

Height

NR3C2 · rs10519959

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Standard

Height (baseline)

near FERD3L · rs10486334

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Standard

Height

near RPSAP1 · rs10485616

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Standard

Height

INSR · rs10415589

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Showing 20 of 10261 · page 125 of 514

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.