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

11,645 positions on this site are linked to Height, out of 2,511,803 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 LINC01808 · rs11886734

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Standard

Height

POLR1HASP · rs3823375

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Height

PRDM16 · rs17822581

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Height

DAAM1 · rs10483713

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Height

near PCSK5 · rs7030848

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Height

LINC01937 · rs10929290

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Standard

Height

LPP · rs938416

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Height

near BMF · rs8023845

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Height

PRKG2 · rs2868140

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Height

AGRN · rs2710888

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Height

MIR4713HG · rs936308

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Height

PCGF5 · rs7069106

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Height

BNC2 · rs10511625

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Height

PTGR2 · rs17782239

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Height

LINC01505 · rs9942977

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Height

YIF1A · rs11544832

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Height

TESHL · rs1179732

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Height

near CDC5L · rs3997520

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Height

GRM4 · rs2229900

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Height

TXNDC5 · rs9502656

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Showing 20 of 11645 · page 33 of 583

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.