Variants linked to Height

Continuously updated · newest added Oct 25, 2026

10,146 positions on this site are linked to Height, out of 116,976 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

TRD-AS1 · rs3811240

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Standard

Height

ZSWIM3 · rs3746524

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Standard

Height

PHAX · rs3734173

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Standard

Height (baseline)

near H19 · rs35936684

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Standard

Height (baseline)

near RPSAP72 · rs34052604

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Standard

Height (baseline)

near LINC02641 · rs34004366

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Standard

Height (baseline)

near C1orf146 · rs3131817

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Standard

Height

near NPM1P21 · rs2953914

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Standard

Height (standard GWA)

NEPRO-AS1 · rs2700227

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Standard

Height

CDK17 · rs2368052

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Standard

Height

near PPARGC1A · rs2324233

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Standard

Height

MKX · rs2253055

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Standard

Height (standard GWA)

SMCHD1 · rs2111679

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Standard

Height (baseline)

TACR3 · rs2086646

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Standard

Height

DLC1 · rs2013653

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Standard

Height (baseline)

ERN1 · rs196919

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Standard

Height (baseline)

ESR1 · rs191357075

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Standard

Height

near Y_RNA · rs1885740

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Standard

Height

SLC17A1 · rs186405009

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Standard

Height (baseline)

near GPX6 · rs184708791

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Showing 20 of 10146 · page 104 of 508

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.