Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,037 positions on this site are linked to Height, out of 2,506,059 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

ZFPM2 · rs1438355

See detailed info → Standard

Height

near LMAN1 · rs12326471

See detailed info → Standard

Height

DAAM2-AS1 · rs11759168

See detailed info → Standard

Height

CCR5AS · rs916093

See detailed info → Standard

Height

PSORS1C1 · rs3778630

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Height

DSCAM · rs2837403

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Height

CHAF1B · rs1906483

See detailed info → Standard

Height

OBSCN · rs4653943

See detailed info → Standard

Height

ST8SIA1 · rs2300726

See detailed info → Standard

Height

near SLC23A4P · rs10954494

See detailed info → Standard

Height (baseline)

near CKB · rs7159665

See detailed info → Standard

Height

near LCORL · rs16896461

See detailed info → Standard

Height

CATSPERB · rs4900084

See detailed info → Standard

Height

near LMAN1 · rs11662962

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Height

near SELENON · rs807245

See detailed info → Standard

Height

SARS2 · rs4803045

See detailed info → Standard

Height

ITPR2-AS2 · rs2129866

See detailed info → Standard

Height

RRP15 · rs11118074

See detailed info → Standard

Height

SOX9-AS1 · rs8077585

See detailed info → Standard

Height

C8orf34 · rs763845

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Showing 20 of 11037 · page 173 of 552

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.