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

11,114 positions on this site are linked to Height, out of 2,506,432 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

FAM3C · rs2254595

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Standard

Height

near RAB1AP2 · rs220428

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Standard

Height

near LINC02503 · rs2134026

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Standard

Height (baseline)

near RN7SL664P · rs189387723

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Standard

Height

LRP2 · rs16856843

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Standard

Height

CREB5 · rs160375

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Standard

Height

MKNK2 · rs1599860

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Standard

Height (baseline)

PRDM12 · rs1545229

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Standard

Height (standard GWA)

near RNU6-500P · rs143973444

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Standard

Height (baseline)

near CMPK1P1 · rs143426188

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Standard

Height

SHC3 · rs1360424

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Standard

Height

C5orf67 · rs13357930

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Standard

Height

near NDUFB4P4 · rs13339876

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Standard

Height

KCNN2 · rs13158827

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Standard

Height

DNM2 · rs12974306

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Standard

Height (standard GWA)

PTPN14 · rs12735790

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Standard

Height

MAX-AS1 · rs1271582

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Standard

Height (baseline)

COL8A1 · rs12487173

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Standard

Height (baseline)

near FBP1 · rs117186988

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Standard

Height

near LINC03007 · rs1159802

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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.