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

11,639 positions on this site are linked to Height, out of 2,511,480 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

PTPN14 · rs4655345

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Standard

Height

NFIC · rs12981408

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Standard

Height

JAZF1 · rs849137

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Standard

Height

ZFAT · rs7829427

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Standard

Height

near U6 · rs763318

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Standard

Height

near H2BC9 · rs6935954

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Standard

Height

ZBTB38 · rs6765238

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Standard

Height

DIS3L2 · rs6437055

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Standard

Height

SOCS2 · rs3825199

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Standard

Height

near HDAC11 · rs2675229

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Standard

Height

RFT1 · rs2581799

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Standard

Height

near NPPC · rs2580816

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Standard

Height

SLC35D2 · rs16910750

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Standard

Height

CTPS1 · rs12408576

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Standard

Height

near CYCSP55 · rs10947487

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Standard

Height

near TBX4 · rs8071653

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Standard

Height

near HLA-DQB1 · rs2395228

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Standard

Height (maximum, inv-normal transformed)

USP36 · rs11649964

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Standard

Height

TCP11 · rs9394274

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Standard

Height

FGD5 · rs4685235

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Showing 20 of 11639 · page 18 of 582

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.