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

10,923 positions on this site are linked to Height, out of 2,505,333 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

CD2AP · rs9369714

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Standard

Height

near DYNLRB2-AS1 · rs4439776

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Standard

Height

KIAA1217 · rs7070056

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Standard

Height

INTS2 · rs8081917

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Standard

Height

PPM1H · rs7302602

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Standard

Height

near LINC02852 · rs1375227

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Standard

Height

ZBTB7C · rs10460075

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Standard

Height

LINC03005 · rs9356834

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Standard

Height

CNIH3 · rs7542507

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Standard

Height

SLC7A8 · rs7157021

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Standard

Height

ZNF618 · rs3827675

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Standard

Height (baseline)

near RPSAP72 · rs28635498

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Standard

Height

DPY19L1 · rs17204148

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Standard

Height

IQSEC1 · rs17037462

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Standard

Height

LTBP1 · rs13427209

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Standard

Height

LINC00970 · rs12048750

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Standard

Height

PPARD · rs9296154

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Standard

Height

DCHS1 · rs7111291

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Standard

Height

C1QTNF7-AS1 · rs2247831

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Standard

Height

FBN1 · rs16960943

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Showing 20 of 10923 · page 148 of 547

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.