Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

10,927 positions on this site are linked to Height, out of 2,505,673 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 (mean, inv-normal transformed)

near RPS3AP24 · rs9399338

See detailed info → Standard

Height

GNAS · rs8121252

See detailed info → Standard

Height

FBLN5 · rs7153027

See detailed info → Standard

Height

ZNF70 · rs145952310

See detailed info → Standard

Standing height (UKB data field 50)

LOXL1 · rs74684534

See detailed info → Standard

Height

BCKDHA · rs4674

See detailed info → Standard

Height

TRIP11 · rs8007661

See detailed info → Standard

Standing height (UKB data field 50)

MSRB3-AS1 · rs58730238

See detailed info → Standard

Standing height (UKB data field 50)

NFATC4 · rs55726184

See detailed info → Standard

Height (baseline)

NR1H3 · rs41275184

See detailed info → Standard

Height

MARK3 · rs17617994

See detailed info → Standard

Height (baseline)

SOCS2-AS1 · rs113043020

See detailed info → Standard

Height

OTUD7B · rs3767627

See detailed info → Standard

Height

TOP1MT · rs2450771

See detailed info → Standard

Height (maximum, inv-normal transformed)

CDCA2 · rs11777745

See detailed info → Standard

Height (maximum, inv-normal transformed)

NAV3 · rs7137768

See detailed info → Standard

Height (baseline)

ANKRD36B · rs55788356

See detailed info → Standard

Height

CALCRL-AS1 · rs17705966

See detailed info → Standard

Height

SPAAR · rs10814297

See detailed info → Standard

Height (maximum, inv-normal transformed)

near LINC01423 · rs9976812

See detailed info →

Showing 20 of 10927 · page 534 of 547

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.