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 11, 2026

11,696 positions on this site are linked to Height, out of 2,512,461 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 (baseline)

CMAHP · rs58657257

See detailed info →
Standard

Height

RPF2 · rs565679040

See detailed info →
Standard

Height (baseline)

COL15A1 · rs55687154

See detailed info →
Standard

Height (baseline)

FBLN5 · rs536493693

See detailed info →
Standard

Height (baseline)

CBX1 · rs533168495

See detailed info →
Standard

Height (baseline)

SAMD3 · rs4897393

See detailed info →
Standard

Height (baseline)

SMARCC1 · rs4858802

See detailed info →
Standard

Height (baseline)

TTC13 · rs4846882

See detailed info →
Standard

Height

COL25A1 · rs4632736

See detailed info →
Standard

Height (baseline)

near LINC02068 · rs446979

See detailed info →
Standard

Height

OSTF1 · rs4376557

See detailed info →
Standard

Height

NR6A1 · rs4073327

See detailed info →
Standard

Height

TRD-AS1 · rs3811240

See detailed info →
Standard

Height

ZSWIM3 · rs3746524

See detailed info →
Standard

Height

PHAX · rs3734173

See detailed info →
Standard

Height (baseline)

near H19 · rs35936684

See detailed info →
Standard

Height (baseline)

near RPSAP72 · rs34052604

See detailed info →
Standard

Height (baseline)

near LINC02641 · rs34004366

See detailed info →
Standard

Height (baseline)

near C1orf146 · rs3131817

See detailed info →
Standard

Height

near NPM1P21 · rs2953914

See detailed info →

Showing 20 of 11696 · page 360 of 585

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.