Variants linked to Height

Continuously updated · newest added Oct 22, 2026

9,248 positions on this site are linked to Height, out of 106,676 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Height

Standard

Height

CUL4A · rs2302755

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Standard

Height (standard GWA)

SLC6A12 · rs2300125

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Standard

Height (baseline)

LOXL2 · rs2294126

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Standard

Height

PCNX1 · rs2286309

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Standard

Height (baseline)

CYP4Z2P · rs192005064

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Standard

Height (baseline)

near FAM153A · rs190279875

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Standard

Height (baseline)

SSTR2 · rs1868486

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Standard

Height (baseline)

DHX30 · rs182599282

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Standard

Height

SOCS5 · rs17822019

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Standard

Height

PALM2AKAP2 · rs17793891

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Standard

Height (standard GWA)

SMAD3 · rs17227883

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Standard

Height

near PPP1R12A-AS1 · rs17006192

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Standard

Height

PHKB · rs16945372

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Standard

Height

near LINC02498 · rs16872454

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Standard

Height

PDE4B · rs1577844

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Standard

Height (standard GWA)

SLC7A1 · rs1571784

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Standard

Height

near KCNIP3 · rs146700697

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Standard

Height (baseline)

near GH1 · rs143499011

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Standard

Height (baseline)

near LINC02823 · rs143014723

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Standard

Height

GPATCH2 · rs12749938

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Showing 20 of 9248 · page 6 of 463

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.