{{Rsnum
|rsid=2293507
|Gene=AUTS2
|Chromosome=7
|position=70763034
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=T
|GMAF=0.07117
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=AUTS2
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 96.5 | 2.7 | 0.9
| HCB | 84.6 | 15.4 | 0.0
| JPT | 91.2 | 8.0 | 0.9
| YRI | 69.4 | 27.9 | 2.7
| ASW | 68.4 | 28.1 | 3.5
| CHB | 84.6 | 15.4 | 0.0
| CHD | 83.5 | 15.6 | 0.9
| GIH | 81.2 | 16.8 | 2.0
| LWK | 75.2 | 22.0 | 2.8
| MEX | 91.4 | 6.9 | 1.7
| MKK | 65.2 | 32.3 | 2.6
| TSI | 89.1 | 10.9 | 0.0
| HapMapRevision=28
}}{{Venter SNP
|rsid=2293507
|allele=T
|frequency=0.033
|uid=1103652606825
|type=heterozygous_SNP
|hugo=AUTS2
|ensembl gene=ENSG00000158321
|ensembl transcript=ENST00000342771
|sift=TOLERATED
|disease=This gene is interrupted by a translocation breakpoint in a pair of autistic twins.
}}

{{GET Evidence
|gene=AUTS2
|aa_change=Ala303Ser
|aa_change_short=A303S
|impact=not reviewed
|qualified_impact=Insufficiently evaluated not reviewed
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2293507
|overall_frequency_n=860
|overall_frequency_d=10758
|overall_frequency=0.0799405
|n_genomes=11
|n_genomes_annotated=0
|n_haplomes=11
|n_articles=0
|n_articles_annotated=0
|nblosum100=-1
|autoscore=0
|webscore=N
}}

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