Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

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.

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Height

Standard

Height

near RNA5SP331 · rs12286771

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Standard

Height

near RPL12P2 · rs12191131

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Standard

Height (baseline)

near LINC02988 · rs12133238

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Standard

Height

LGR6 · rs12123327

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Standard

Height

XXYLT1 · rs11919965

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Standard

Height

PRKG1 · rs1189316

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Standard

Height (baseline)

AOPEP · rs118154071

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Standard

Height (baseline)

SEC24A · rs11748298

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Standard

Height (baseline)

RNA5SP126 · rs11712065

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Standard

Height

RBMS3 · rs11710772

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Standard

Height

FOXP1 · rs11709093

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Standard

Height (baseline)

near LINC02872 · rs116852201

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Standard

Height (baseline)

SLC38A9 · rs116741620

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Height

COX10-DT · rs11651178

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Height

LPXN · rs11605297

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Standard

Height (baseline)

FBXW11 · rs116003693

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Standard

Height (baseline)

ANKS1A · rs114046576

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Standard

Height (baseline)

C9orf163 · rs1139057

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Standard

Height

SLC12A6 · rs1133154

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Height

SFMBT2 · rs11255049

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Showing 20 of 11146 · page 378 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.