Gene Knowledge Graph
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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 2,506,722 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)

FAM53B · rs7917674

See detailed info → Standard

height (mean, inv-normal transformed)

near U3 · rs73279106

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Height

near RN7SL480P · rs956796

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height (minimum, inv-normal transformed)

TRPC3 · rs72680779

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Height (maximum, inv-normal transformed)

TNRC6A · rs7184364

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Height

MIR99AHG · rs12483653

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Height

ZC3HAV1 · rs7811342

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height (mean, inv-normal transformed)

near RNU6-778P · rs6695240

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Height (maximum, inv-normal transformed)

near RPS19P6 · rs4877619

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height (minimum, inv-normal transformed)

TRIM41 · rs2770957

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Height

TLR9 · rs352140

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Height (baseline)

DLEU1 · rs2740510

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height (mean, inv-normal transformed)

FHIP1A-DT · rs2724553

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Standing height (UKB data field 50)

LINC02742 · rs7928703

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height (mean, inv-normal transformed)

near PIK3R1 · rs453940

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Height (baseline)

ADAMTS17 · rs4338785

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Height

PNRC1 · rs1130809

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Height

SPTY2D1 · rs10832962

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height (mean, inv-normal transformed)

near POLR3A · rs12218917

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Height

ZFHX3 · rs6564524

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Showing 20 of 11146 · page 216 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.