{{Rsnum
|rsid=879471
|Gene=STMN3
|Chromosome=20
|position=63638589
|Orientation=plus
|GMAF=0.3407
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 22.5 | 42.3 | 35.1
| HCB | 79.4 | 16.9 | 3.7
| JPT | 80.5 | 15.9 | 3.5
| YRI | 73.1 | 22.1 | 4.8
| ASW | 45.6 | 47.4 | 7.0
| CHB | 79.4 | 16.9 | 3.7
| CHD | 78.0 | 21.1 | 0.9
| GIH | 60.0 | 35.0 | 5.0
| LWK | 68.8 | 26.6 | 4.6
| MEX | 43.9 | 45.6 | 10.5
| MKK | 47.4 | 41.7 | 10.9
| TSI | 17.6 | 46.1 | 36.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=23091480
|Title=Leveraging ethnic group incidence variation to investigate genetic susceptibility to glioma: a novel candidate SNP approach
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}
{{on chip | NatGeo2}}