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 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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 EYA4 · rs6902399

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Standard

Height

LINC02641 · rs6599698

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Standard

Height (baseline)

MIATNB · rs6005256

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Standard

Height

LINC02550 · rs534858

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Standard

Height (baseline)

near ZNF322 · rs533455911

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Standard

Height

near TPT1P9 · rs516489

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Standard

Height

MYO16-AS1 · rs496313

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Standard

Height (baseline)

STK10 · rs4867663

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Standard

Height

TTLL4 · rs4674332

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Standard

Height

CLUAP1 · rs3751836

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Standard

Height

SLC52A3 · rs3746804

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Standard

Height (baseline)

DISP1 · rs36198151

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Standard

Height

FBN1 · rs200342067

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Standard

Height (baseline)

WNT6 · rs190613671

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Standard

Height (baseline)

CAMKMT · rs17498998

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Standard

Height

near RNU7-34P · rs17144556

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Standard

Height

DDAH1 · rs17099679

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Standard

Height

MAP4K4 · rs17026163

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Standard

Height (baseline)

near SLC66A1LP · rs140875643

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Standard

Height (baseline)

DYM-AS1 · rs140278307

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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.