Gene Knowledge Graph
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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 9, 2026

11,375 positions on this site are linked to Height, out of 2,508,671 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height (baseline)

LIN28B-AS1 · rs10485310

See detailed info → Standard

Height (baseline)

EFEMP1 · rs727877

See detailed info → Standard

Height (baseline)

MEPE · rs727421

See detailed info → Standard

Height

LAMA4-AS1 · rs6931341

See detailed info → Standard

Height

ZNRF3-IT1 · rs5997427

See detailed info → Standard

Height

LRCH3 · rs538885

See detailed info → Standard

Height (baseline)

CREB5 · rs4722835

See detailed info → Standard

Height

near LINC01973 · rs4633782

See detailed info → Standard

Height

near SP8 · rs34661314

See detailed info → Standard

Height

near LIMK1 · rs34325097

See detailed info → Standard

Height

MEG9 · rs2295655

See detailed info → Standard

Height

PDE4B · rs1937456

See detailed info → Standard

Height (baseline)

MLF1-DT · rs1656374

See detailed info → Standard

Height

ERGIC1 · rs9313609

See detailed info → Standard

Height

ZBED5-AS1 · rs771373

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

HEXIM2-AS1 · rs76233987

See detailed info → Standard

Height

CFAP54 · rs2111146

See detailed info → Standard

Height

CDH9 · rs17566929

See detailed info → Standard

Height

ARL15 · rs16881847

See detailed info → Standard

Height

SGCD · rs10057826

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Showing 20 of 11375 · page 520 of 569

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.