Gene Knowledge Graph

UTC

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

11,159 positions on this site are linked to Height, out of 2,506,771 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

Height

near LINC01893 · rs961560

See detailed info → Standard

Height

TDRG1 · rs9471290

See detailed info → Standard

Height

near NUP50P4 · rs9447339

See detailed info → Standard

Height

near NPAP1L · rs9302724

See detailed info → Standard

Height

near RNU6-660P · rs904752

See detailed info → Standard

Height

CMIP · rs876672

See detailed info → Standard

Height

near ZNF429 · rs8112960

See detailed info → Standard

Height

PSEN1 · rs8006497

See detailed info → Standard

Height

near MTND2P8 · rs7875186

See detailed info → Standard

Height

NR6A1 · rs7868877

See detailed info → Standard

Height (baseline)

near SPATA31C2 · rs78504486

See detailed info → Standard

Height (baseline)

near SLC23A4P · rs7793333

See detailed info → Standard

Height (baseline)

TRAK2 · rs7592494

See detailed info → Standard

Height

KREMEN1 · rs7289560

See detailed info → Standard

height (mean, inv-normal transformed)

PPM1G · rs72819512

See detailed info → Standard

Height

C1QTNF1 · rs7213410

See detailed info → Standard

Height

near VPS33B-DT · rs7175820

See detailed info → Standard

Height (baseline)

CASC9 · rs71527286

See detailed info → Standard

Height (baseline)

TTLL4 · rs71415857

See detailed info → Standard

Height (baseline)

near GAPDHP72 · rs705821

See detailed info →

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.