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

11,607 positions on this site are linked to Height, out of 2,511,197 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

CLCN3 · rs1010713

See detailed info →
Standard

Height

PDE7B · rs9494412

See detailed info →
Standard

Height

near SENP2 · rs9290822

See detailed info →
Standard

Height

RNF111 · rs8037652

See detailed info →
Standard

Height

near SOCS2 · rs7971647

See detailed info →
Standard

Height (baseline)

ANAPC10 · rs78687227

See detailed info →
Standard

Height

DLC1 · rs7834479

See detailed info →
Standard

Height

near TMEM167A · rs7717856

See detailed info →
Standard

Height (baseline)

near HIVEP2 · rs75109124

See detailed info →
Standard

Height (baseline)

NF1 · rs7503951

See detailed info →
Standard

Height (baseline)

near NPR3 · rs72742745

See detailed info →
Standard

Height

TANC2 · rs7211831

See detailed info →
Standard

Standing height (UKB data field 50)

SMAD3-DT · rs7162222

See detailed info →
Standard

Height

BTC · rs6840529

See detailed info →
Standard

Height

PLXNA2 · rs4844642

See detailed info →
Standard

Height

KCNK15-AS1 · rs4812851

See detailed info →
Standard

Height

near LDHAP1 · rs4689961

See detailed info →
Standard

Height

FAM47E-STBD1 · rs3733251

See detailed info →
Standard

Height (baseline)

MYO9A · rs2929513

See detailed info →
Standard

Height

RGS7 · rs2815834

See detailed info →

Showing 20 of 11607 · page 518 of 581

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.