{{Rsnum
|rsid=6469937
|Gene=SNTB1
|Chromosome=8
|position=120598198
|Orientation=plus
|GMAF=0.3972
|Gene_s=SNTB1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 38.9 | 52.2 | 8.8
| HCB | 5.8 | 43.8 | 50.4
| JPT | 1.8 | 36.6 | 61.6
| YRI | 2.7 | 25.2 | 72.1
| ASW | 8.8 | 29.8 | 61.4
| CHB | 5.8 | 43.8 | 50.4
| CHD | 11.0 | 37.6 | 51.4
| GIH | 19.8 | 43.6 | 36.6
| LWK | 1.8 | 20.9 | 77.3
| MEX | 19.3 | 49.1 | 31.6
| MKK | 1.9 | 29.5 | 68.6
| TSI | 40.2 | 42.2 | 17.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23933737
  |Trait=Myopia (severe)
  |Title=Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.
  |RiskAllele=A
  |Pval=2E-9
  |OR=1.27
  |ORtxt=[NR]
  }}

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