Gene Knowledge Graph
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Variants linked to Height

Continuously updated · newest added Nov 10, 2026

11,491 positions on this site are linked to Height, out of 2,509,608 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)

GRB2 · rs28488378

See detailed info → Standard

Height

LINC03138 · rs2831703

See detailed info → Standard

Height (baseline)

near RN7SL554P · rs2802415

See detailed info → Standard

Height

near RNA5SP228 · rs272693

See detailed info → Standard

Height

LPCAT1 · rs27051

See detailed info → Standard

Height (baseline)

POLR1HASP · rs259942

See detailed info → Standard

Height (baseline)

FIG4 · rs2492979

See detailed info → Standard

Height (baseline)

LINC01713 · rs235735

See detailed info → Standard

Height

POLR3E · rs201672353

See detailed info → Standard

Height

near LINC01991 · rs2009627

See detailed info → Standard

Height

near XRCC6P1 · rs1927465

See detailed info → Standard

Height

near U3 · rs17048207

See detailed info → Standard

Height

LAPTM4A-DT · rs16987337

See detailed info → Standard

Height (baseline)

FBXO27 · rs1654336

See detailed info → Standard

Height (baseline)

ADAMTSL3 · rs148298313

See detailed info → Standard

Height (baseline)

LMX1B-DT · rs147961605

See detailed info → Standard

Height (baseline)

NEO1 · rs147221393

See detailed info → Standard

Height (baseline)

near RNA5SP214 · rs145833963

See detailed info → Standard

Height (standard GWA)

FILIP1 · rs145206747

See detailed info → Standard

Height (baseline)

near RPL34-DT · rs141852021

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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.