{{Rsnum
|rsid=397514705
|Chromosome=22
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=SHANK3
|position=50678666
|Gene_s=SHANK3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=22
|CLNACC=RCV000043655.1
|CLNALLE=1
|CLNDBN=22q13.3 deletion syndrome
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1198:C1853490:606232:48652
|CLNHGVS=NC_000022.10:g.51117094C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606230.0006
|Disease=22q13.3 deletion syndrome
|FwdALT=G
|FwdREF=C
|GENEINFO=SHANK3:85358
|GENE_ID=85358
|GENE_NAME=SHANK3
|REF=C
|RSPOS=51117094
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514705
}}