{{Rsnum
|rsid=137853127
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SATB2
|position=199349159
|Gene_s=SATB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608148
|variant=0001
|rsnum=137853127
}}{{ClinVar
|rsid=137853127
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=200213882
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SATB2:23314
|GENE_NAME=SATB2
|GENE_ID=23314
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.200213882G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000002627.2
|CLNDBN=Chromosome 2q32-q33 deletion syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2676739:612313:251019
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608148.0001
|Disease=Chromosome 2q32-q33 deletion syndrome
}}