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 10, 2026

11,487 positions on this site are linked to Height, out of 2,509,560 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

PCNX1 · rs2286309

See detailed info → Standard

Height (baseline)

CYP4Z2P · rs192005064

See detailed info → Standard

Height (baseline)

near FAM153A · rs190279875

See detailed info → Standard

Height (baseline)

SSTR2 · rs1868486

See detailed info → Standard

Height (baseline)

DHX30 · rs182599282

See detailed info → Standard

Height

SOCS5 · rs17822019

See detailed info → Standard

Height

PALM2AKAP2 · rs17793891

See detailed info → Standard

Height (standard GWA)

SMAD3 · rs17227883

See detailed info → Standard

Height

near PPP1R12A-AS1 · rs17006192

See detailed info → Standard

Height

PHKB · rs16945372

See detailed info → Standard

Height

near LINC02498 · rs16872454

See detailed info → Standard

Height

PDE4B · rs1577844

See detailed info → Standard

Height (standard GWA)

SLC7A1 · rs1571784

See detailed info → Standard

Height

near KCNIP3 · rs146700697

See detailed info → Standard

Height (baseline)

near GH1 · rs143499011

See detailed info → Standard

Height (baseline)

near LINC02823 · rs143014723

See detailed info → Standard

Height

GPATCH2 · rs12749938

See detailed info → Standard

Height

KALRN · rs12695436

See detailed info → Standard

Height

near CYB5AP3 · rs12589195

See detailed info → Standard

Height (baseline)

FGGY · rs12568514

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.