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 12, 2026

11,879 positions on this site are linked to Height, out of 2,515,865 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)

FAM184B · rs111648780

See detailed info → Standard

Height

near RHOB · rs1010415

See detailed info → Standard

Height

LARGE1 · rs1005680

See detailed info → Standard

Height

RPL26L1 · rs9784719

See detailed info → Standard

Height (baseline)

EML6 · rs9751102

See detailed info → Standard

Height

GIGYF2 · rs894857163

See detailed info → Standard

Height (baseline)

near CRADD · rs80307446

See detailed info → Standard

Height (baseline)

FLYWCH2 · rs79424176

See detailed info → Standard

Height (baseline)

KLHL29 · rs78926083

See detailed info → Standard

Height (baseline)

near SMG1P5 · rs77016006

See detailed info → Standard

Height (baseline)

PNPLA1 · rs76228061

See detailed info → Standard

Height

PTBP2 · rs7513314

See detailed info → Standard

Height (baseline)

THRB-AS2 · rs74956157

See detailed info → Standard

Height

FHAD1 · rs736185

See detailed info → Standard

Height (baseline)

IGF1 · rs73180982

See detailed info → Standard

Height (baseline)

ACAN · rs72765681

See detailed info → Standard

Height

LINC01081 · rs7201739

See detailed info → Standard

Height (baseline)

CCND2-AS1 · rs71458092

See detailed info → Standard

Height (baseline)

LIN28B · rs6902142

See detailed info → Standard

Height (baseline)

SLC7A15P · rs6531236

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Showing 20 of 11879 · page 359 of 594

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.