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.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Height (maximum, inv-normal transformed)

LPAR6 · rs59128343

See detailed info → Standard

height (mean, inv-normal transformed)

near JCAD · rs2140427

See detailed info → Standard

Standing height (UKB data field 50)

ESR1 · rs35882398

See detailed info → Standard

Standing height (UKB data field 50)

PHF11 · rs77929895

See detailed info → Standard

Standing height (UKB data field 50)

RTL1 · rs6575805

See detailed info → Standard

Height (baseline)

near DRAP1 · rs589253

See detailed info → Standard

What is your height? (cm, inv-normal transformed)

SP3 · rs116283900

See detailed info → Standard

Height (baseline)

AFG1L · rs9486879

See detailed info → Standard

height (mean, inv-normal transformed)

near XRCC1 · rs2682558

See detailed info → Standard

height (mean, inv-normal transformed)

SCAPER · rs62029233

See detailed info → Standard

Height

BBX · rs600011

See detailed info → Standard

Height

NFRKB · rs1650823

See detailed info → Standard

Height

COX19 · rs7792825

See detailed info → Standard

Height (maximum, inv-normal transformed)

RAD51B · rs17192558

See detailed info → Standard

Height

LSAMP · rs9790189

See detailed info → Standard

Height

DCST1 · rs76306191

See detailed info → Standard

Standing height (UKB data field 50)

SLC27A6 · rs188023348

See detailed info → Standard

Height

CDK6-AS1 · rs10269570

See detailed info → Standard

Height (baseline)

near LINC02127 · rs34652933

See detailed info → Standard

Standing height (UKB data field 50)

near FGFR4 · rs141774838

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.