Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,037 positions on this site are linked to Height, out of 2,506,059 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

near H3P27 · rs1414595

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Standard

Height

near LINC01159 · rs7579394

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Standard

Height

ITPKB · rs708775

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Standard

Height

near ADIPOR1P1 · rs34737777

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Standard

Height

PPIA · rs17134462

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Standard

Height

near LINC02952 · rs11263451

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Standard

height (minimum, inv-normal transformed)

PCSK5 · rs13294753

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Standard

Height

PPP6R3 · rs11228271

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Standard

Height

CHST11 · rs11112153

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Standard

Height

BMP6 · rs267194

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Standard

Height

LINC02032 · rs1456671

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Standard

Height

LINC02934 · rs13384003

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Standard

Height

NPR3 · rs1173737

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Standard

Height

FGGY · rs11207439

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Standard

Height

PARN · rs7501119

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Standard

Height

ARID4B · rs12036412

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Standard

Height

LINC01991 · rs498688

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Standard

Height

near HMGN1 · rs2836989

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Standard

Height

KIAA0753 · rs2165844

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Standard

Height

IGF2BP3 · rs17740440

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Showing 20 of 11037 · page 172 of 552

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.