Gene Knowledge Graph

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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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 (standard GWA)

EFCAB5 · rs114658410

See detailed info → Standard

Height

near LINC01519 · rs11201527

See detailed info → Standard

Height

SPSB1 · rs11121380

See detailed info → Standard

Height

near RPSAP20 · rs10888959

See detailed info → Standard

Height (baseline)

SYN3 · rs10854622

See detailed info → Standard

Height (baseline)

GRB10 · rs10235705

See detailed info → Standard

Height

ADCY1 · rs10225980

See detailed info → Standard

Height

near SBF1P2 · rs1009592

See detailed info → Standard

Gluteofemoral adipose tissue volumes (adjusted for BMI and height)

LINC02227 · rs10044492

See detailed info → Standard

Height

LINC01725 · rs9787364

See detailed info → Standard

Height

ANO1 · rs9630219

See detailed info → Standard

Height (baseline)

near LNX2 · rs9581878

See detailed info → Standard

Height

BMP6 · rs9505276

See detailed info → Standard

Height (baseline)

near HMGN1P19 · rs856586

See detailed info → Standard

Height

ETS2-AS1 · rs8131592

See detailed info → Standard

Height (baseline)

LINC01574 · rs812817

See detailed info → Standard

Height

WFDC1 · rs8051764

See detailed info → Standard

Height

GALNT1 · rs79641095

See detailed info → Standard

Height

near Y_RNA · rs7902725

See detailed info → Standard

Height (standard GWA)

near RPS26 · rs78865465

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.