Gene Knowledge Graph

UTC

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 11, 2026

11,696 positions on this site are linked to Height, out of 2,512,461 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

Height (standard GWA)

NEPRO-AS1 · rs2700227

See detailed info → Standard

Height

CDK17 · rs2368052

See detailed info → Standard

Height

near PPARGC1A · rs2324233

See detailed info → Standard

Height

MKX · rs2253055

See detailed info → Standard

Height (standard GWA)

SMCHD1 · rs2111679

See detailed info → Standard

Height (baseline)

TACR3 · rs2086646

See detailed info → Standard

Height

DLC1 · rs2013653

See detailed info → Standard

Height (baseline)

ERN1 · rs196919

See detailed info → Standard

Height (baseline)

ESR1 · rs191357075

See detailed info → Standard

Height

near Y_RNA · rs1885740

See detailed info → Standard

Height

SLC17A1 · rs186405009

See detailed info → Standard

Height (baseline)

near GPX6 · rs184708791

See detailed info → Standard

Height (baseline)

LYPLAL1-DT · rs17578870

See detailed info → Standard

Height

near RN7SKP65 · rs17492213

See detailed info → Standard

Height

near DPPA3P11 · rs17350321

See detailed info → Standard

Height

near RPL18AP17 · rs17089074

See detailed info → Standard

Height

NCALD · rs16868803

See detailed info → Standard

Height (baseline)

near BMP6 · rs150849052

See detailed info → Standard

Height (baseline)

FEZ2 · rs147763767

See detailed info → Standard

Height

near HNRNPA1P64 · rs145685136

See detailed info →

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.