Gene Knowledge Graph
UTC

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Variants linked to Height

Continuously updated · newest added Nov 8, 2026

11,146 positions on this site are linked to Height, out of 2,506,627 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 (baseline)

near LINC02412 · rs112082543

See detailed info → Standard

Height (baseline)

SYNM-AS1 · rs111563582

See detailed info → Standard

Height (standard GWA)

PRKG1 · rs10997777

See detailed info → Standard

Height

PRKG1 · rs10995339

See detailed info → Standard

Height

near SPAG17 · rs10923510

See detailed info → Standard

Height (baseline)

near BAMBI · rs10826494

See detailed info → Standard

Height

UNC80 · rs10804178

See detailed info → Standard

Height

RASSF8 · rs10771251

See detailed info → Standard

Height

DTNA · rs10502634

See detailed info → Standard

Height

near NOVA1 · rs10498286

See detailed info → Standard

Height

MFSD12-AS1 · rs10424296

See detailed info → Standard

Height

POU2F1 · rs1028703

See detailed info → Standard

Height

near NDUFS6P1 · rs10212532

See detailed info → Standard

Height

UGGT1 · rs10180829

See detailed info → Standard

Height

near MSNP1 · rs10065041

See detailed info → Standard

Height

ZNF518B · rs10021506

See detailed info → Standard

Height

LPCAT3 · rs9668071

See detailed info → Standard

Height

MGST1 · rs9332884

See detailed info → Standard

Height

MAPK1 · rs8136867

See detailed info → Standard

Standing height (UKB data field 50)

near HMGB3P2 · rs80079105

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Showing 20 of 11146 · page 379 of 558

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.