Gene Knowledge Graph
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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.

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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

CXXC5 · rs73790670

See detailed info → Standard

Height (baseline)

near LINC02161 · rs72656671

See detailed info → Standard

Height

DLG2 · rs7119459

See detailed info → Standard

Height

DDR2 · rs6702820

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Height

near RNU7-14P · rs6022643

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Height (baseline)

GORASP2 · rs5836311

See detailed info → Standard

Height (standard GWA)

near RPS27P12 · rs58157417

See detailed info → Standard

Height (baseline)

FANCA · rs541408613

See detailed info → Standard

Height

LINC01215 · rs4855619

See detailed info → Standard

Height

near ERCC6L2-AS1 · rs4743291

See detailed info → Standard

Height (baseline)

DRAM1 · rs4517576

See detailed info → Standard

Height (baseline)

ST8SIA1 · rs3819876

See detailed info → Standard

Height

PKN1 · rs3786654

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Height

POLD3 · rs3741127

See detailed info → Standard

Height

RETREG1 · rs31289

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Height (baseline)

near VDAC2P3 · rs28571583

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Height

near MED6P1 · rs2673824

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Height

CUL4A · rs2302755

See detailed info → Standard

Height (standard GWA)

SLC6A12 · rs2300125

See detailed info → Standard

Height (baseline)

LOXL2 · rs2294126

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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.