{{Rsnum
|rsid=137852982
|Chromosome=2
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ZEB2
|position=144398632
|Gene_s=ZEB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=605802
|variant=0009
|rsnum=137852982
}}{{ClinVar
|rsid=137852982
|Reversed=1
|FwdREF=C
|FwdALT=G
|REF=G
|ALT=C
|RSPOS=145156199
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ZEB2:9839
|GENE_NAME=ZEB2
|GENE_ID=9839
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.145156199G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605802.0009
|CLNSIG=5
|CLNCUI=C1856113
|CLNDBN=Mowat-Wilson syndrome
|Disease=Mowat-Wilson syndrome
|CLNACC=RCV000005028.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1412:C1856113:235730:2152
}}