{{Rsnum
|rsid=4557020
|Gene=SPTBN1
|Chromosome=2
|position=54491044
|Orientation=plus
|GMAF=0.3848
|Gene_s=SPTBN1
|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 | 19.5 | 54.0 | 26.5
| HCB | 43.1 | 40.9 | 16.1
| JPT | 29.2 | 56.6 | 14.2
| YRI | 77.6 | 20.4 | 2.0
| ASW | 50.9 | 43.9 | 5.3
| CHB | 43.1 | 40.9 | 16.1
| CHD | 35.8 | 49.5 | 14.7
| GIH | 37.6 | 43.6 | 18.8
| LWK | 80.9 | 17.3 | 1.8
| MEX | 37.9 | 32.8 | 29.3
| MKK | 64.1 | 31.4 | 4.5
| TSI | 21.6 | 42.2 | 36.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22685421
|Trait=None
|Title=Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.
|RiskAllele=T
|Pval=3E-7
|OR=0.1200
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}