{{Rsnum
|rsid=10174126
|Gene=SH3BP4
|Chromosome=2
|position=235052249
|Orientation=plus
|GMAF=0.4247
|Gene_s=SH3BP4
|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 | 25.7 | 47.8 | 26.5
| HCB | 49.6 | 38.7 | 11.7
| JPT | 56.6 | 34.5 | 8.8
| YRI | 53.1 | 38.8 | 8.2
| ASW | 47.4 | 40.4 | 12.3
| CHB | 49.6 | 38.7 | 11.7
| CHD | 47.2 | 42.6 | 10.2
| GIH | 44.6 | 45.5 | 9.9
| LWK | 39.1 | 48.2 | 12.7
| MEX | 17.2 | 39.7 | 43.1
| MKK | 31.6 | 47.7 | 20.6
| TSI | 24.5 | 52.0 | 23.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22419666
|Trait=None
|Title=Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.
|RiskAllele=
|Pval=7E-7
|OR=1.5900
|ORtxt=None
|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}}