{{Rsnum
|rsid=9616915
|Gene=SHANK3
|Chromosome=22
|position=50679152
|Orientation=plus
|GMAF=0.3581
|Gene_s=SHANK3
|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 | 23.1 | 51.9 | 25.0
| HCB | 1.5 | 16.1 | 82.5
| JPT | 1.8 | 26.5 | 71.7
| YRI | 12.1 | 51.1 | 36.9
| ASW | 12.3 | 54.4 | 33.3
| CHB | 1.5 | 16.1 | 82.5
| CHD | 0.0 | 13.8 | 86.2
| GIH | 22.0 | 45.0 | 33.0
| LWK | 15.9 | 50.5 | 33.6
| MEX | 7.0 | 38.6 | 54.4
| MKK | 27.7 | 45.2 | 27.1
| TSI | 29.6 | 37.8 | 32.7
| HapMapRevision=28
}}{{PMID Auto
|PMID=24398551
|Title=A commonly carried genetic variant, rs9616915, in SHANK3 gene is associated with a reduced risk of autism spectrum disorder: replication in a Chinese population
}}

{{PMID Auto
|PMID=19384346
|Title=Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection.
|OA=1
}}

{{PMID Auto
|PMID=19566951
|Title=Association study of SHANK3 gene polymorphisms with autism in Chinese Han population.
|OA=1
}}

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