Gene Knowledge Graph
UTC

Variants linked to Height

Continuously updated · newest added Oct 24, 2026

9,869 positions on this site are linked to Height, out of 113,447 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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Standard

Height (maximum, inv-normal transformed)

near ADAMTS2 · rs7722790

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Height (baseline)

PNPT1 · rs76693423

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Height (baseline)

CTPS1 · rs72663737

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Height

SLC22A1 · rs594709

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Height (baseline)

FANCC · rs549658720

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Height (baseline)

LIN28A · rs35184161

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Height (baseline)

FER · rs35137434

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Height (baseline)

PDE3A · rs76274569

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Standing height (UKB data field 50)

PCSK5 · rs3739728

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Height (baseline)

DDX42 · rs150030396

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Height (baseline)

CRLF3 · rs141870697

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Height (baseline)

ATP6V1E2 · rs13008445

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Height (baseline)

ZNF892 · rs113996403

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Height (maximum, inv-normal transformed)

near AVPR1A · rs11174852

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Height

ZNF143 · rs10770035

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Height (baseline)

HMGA2 · rs73121706

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Height (baseline)

CBFA2T2 · rs73119111

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Height (baseline)

near HLA-DQA1 · rs534868470

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Height

KCNJ12 · rs4488509

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Height (baseline)

SAPCD1-AS1 · rs28399993

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Showing 20 of 9869 · page 425 of 494

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.