Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,114 positions on this site are linked to Height, out of 2,506,432 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

PDE4D · rs2963826

See detailed info → Standard

Height

KMT2D · rs2241726

See detailed info → Standard

Height (baseline)

TESHL · rs2241192

See detailed info → Standard

Height (baseline)

near QKI · rs2104232

See detailed info → Standard

Height

DLEU1 · rs2066664

See detailed info → Standard

Height

near SLC6A9 · rs1978195

See detailed info → Standard

Height

PTHLH · rs1974747

See detailed info → Standard

Height

near PPIAP88 · rs1962035

See detailed info → Standard

Height (baseline)

near LINC02503 · rs189568747

See detailed info → Standard

Height (baseline)

MYOZ2 · rs187690620

See detailed info → Standard

Height (baseline)

DYSF · rs181511706

See detailed info → Standard

Height

MYO1D · rs17806495

See detailed info → Standard

Height (baseline)

ENTPD4 · rs17696480

See detailed info → Standard

Height

CLEC16A · rs17673553

See detailed info → Standard

Height

BRD3 · rs17566226

See detailed info → Standard

Height

IPPK · rs17366134

See detailed info → Standard

Height

near OSBPL8 · rs17199131

See detailed info → Standard

Height

RPL7AP9 · rs17042412

See detailed info → Standard

Height

near SMAD7 · rs16950087

See detailed info → Standard

Height

STAU2 · rs16938648

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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.