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 9, 2026

11,272 positions on this site are linked to Height, out of 2,507,630 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 (maximum, inv-normal transformed)

near MIR3622B · rs566398

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Standard

Height (baseline)

ATP9A · rs55722823

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Standard

Height (baseline)

SLX1A-SULT1A3 · rs532388992

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Standard

Height

near RDX · rs4753885

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Standard

Height

near RGMA · rs4396487

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Standard

Height

near RNU2-54P · rs41373546

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Standard

Height (baseline)

CCDC127 · rs3932940

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Standard

Height

DYNC1I2 · rs3796000

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Standard

Height

OBI1-AS1 · rs2806592

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Standard

Height

near XXYLT1 · rs2676834

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Standard

Height

near U6 · rs2540843

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Standard

Height

MEGF9 · rs2416760

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Standard

Height (baseline)

near BMP6 · rs2327013

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Standard

Height (baseline)

BCL9 · rs2132441

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Standard

Height

near DHX35 · rs2103613

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Standard

Height (baseline)

near DDX10P2 · rs2038995

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Standard

Height

FRYL · rs1996422

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Standard

Height (standard GWA)

near CD2AP-DT · rs1931833

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Standard

Height (baseline)

near IGKV2-26 · rs187801408

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Standard

Height

KAT2B · rs186900581

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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.