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

GFRA1 · rs2694765

See detailed info → Standard

Height

SLC2A13 · rs28370628

See detailed info → Standard

Height

near IMPA2 · rs2849412

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Height

GHRHR · rs28710006

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Height

near ZNF648 · rs3856113

See detailed info → Standard

Height

TTC23L · rs3857367

See detailed info → Standard

Height

RALGPS1 · rs4292797

See detailed info → Standard

Height

SSBP2 · rs434078

See detailed info → Standard

Height

GPC6 · rs4773767

See detailed info → Standard

Height

SLC9A4 · rs4851596

See detailed info → Standard

Height

HECW2 · rs540884507

See detailed info → Standard

Height

near ZNF611 · rs541803728

See detailed info → Standard

Height

RERGL · rs552712403

See detailed info → Standard

Height

CRIP1 · rs55633823

See detailed info → Standard

Height

ITGB5 · rs62265658

See detailed info → Standard

Height

near TTC14 · rs62290978

See detailed info → Standard

Height

LARP7 · rs62317770

See detailed info → Standard

Height

MMP16 · rs62525862

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Height

near CALCRL · rs6434213

See detailed info → Standard

Height

KANSL1L · rs6435550

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Showing 20 of 10927 · page 538 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.