Variants linked to Height

Continuously updated · newest added Oct 23, 2026

9,705 positions on this site are linked to Height, out of 111,393 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

DYNC1I1 · rs940424

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Standard

Height

RNF217 · rs9401790

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Standard

Height

TRAM2 · rs9382120

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Standard

Height

near FAM136FP · rs9343143

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Standard

Height (baseline)

near PPM1A · rs9323363

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Standard

Height

BICD2 · rs912262

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Standard

Height (baseline)

near ARF3 · rs833826

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Standard

Height (baseline)

near BTF3P7 · rs80156790

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Standard

Height

near LINC01048 · rs7992372

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Standard

Height (baseline)

SLC38A9 · rs79560556

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Standard

Height (baseline)

MIR100HG · rs7937427

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Standard

Height

TTC17 · rs7937002

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Standard

Height

near FAM76B · rs7927955

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Standard

Height (baseline)

PMPCA · rs79265255

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Standard

Height (baseline)

FNDC3A · rs78871791

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Standard

Height (baseline)

PRSS42P · rs78629618

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Standard

Height (baseline)

COLGALT2 · rs77960807

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Standard

Height (baseline)

CPZ · rs77855174

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Standard

Height (baseline)

near FOXO6 · rs77598229

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Standard

Height (baseline)

near RN7SKP211 · rs7750292

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Showing 20 of 9705 · page 48 of 486

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.