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 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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)

near NCOA1 · rs13395245

See detailed info → Standard

Height

near IGFBP3 · rs13232606

See detailed info → Standard

Height (baseline)

ITPR3 · rs13219530

See detailed info → Standard

Height

near LINC01702 · rs12756945

See detailed info → Standard

Height

COL11A1 · rs12046389

See detailed info → Standard

Height (baseline)

MTCH2 · rs113359244

See detailed info → Standard

Height

HYI-AS1 · rs11210843

See detailed info → Standard

Height

CACNA1C · rs11062066

See detailed info → Standard

Height

PATJ · rs10889253

See detailed info → Standard

Height

LRRC8A · rs941959

See detailed info → Standard

Height

PLUT · rs7981979

See detailed info → Standard

Height (baseline)

near TENT5A · rs75819056

See detailed info → Standard

Height

ITPKB · rs708772

See detailed info → Standard

Height

ZNF516 · rs689902

See detailed info → Standard

Height (baseline)

GNA12 · rs540524389

See detailed info → Standard

Height

SMG7 · rs41439047

See detailed info → Standard

Height

MARCHF10 · rs3901444

See detailed info → Standard

Height (baseline)

CLIP1 · rs34292795

See detailed info → Standard

Height

ZFP82 · rs2945989

See detailed info → Standard

Height

SLC38A4-AS1 · rs2075335

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Showing 20 of 11491 · page 367 of 575

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.