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 11, 2026

11,668 positions on this site are linked to Height, out of 2,512,094 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

LAMA3 · rs11662490

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Height

near RNU4ATAC6P · rs12411515

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Height

ARHGAP24 · rs1823762

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Height

CHSY1 · rs11638414

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Height

near PRELID3B · rs4810150

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Height

near LINC02997 · rs17318106

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Height

NSD1 · rs11953271

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Height

near NPPC · rs7588259

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Height

BSX · rs11218912

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Height

near PCAT7 · rs11998973

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Height

CAMKMT · rs343962

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Height

TNPO1-DT · rs2338637

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Height

near RN7SL316P · rs7209032

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Height

near NAB1 · rs2356121

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Height

near PTCH1 · rs16909859

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Height

near SYNDIG1L · rs7156302

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Height

TMX2 · rs36036499

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Height

RREB1 · rs2326883

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Height

near GBP3 · rs6428494

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Height

DMP1-AS1 · rs10016081

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Showing 20 of 11668 · page 53 of 584

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.