{{Rsnum
|rsid=367543070
|Chromosome=1
|position=235489220
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TG)
|geno3=(TG;TG)
|Gene=B3GALNT2
|Gene_s=B3GALNT2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000034846.4
|CLNALLE=1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A11
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN168979:615181:588:899
|CLNHGVS=NC_000001.10:g.235652525_235652526delCA
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=610194.0003
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdREF=TG
|REF=CCA
|RSPOS=235652524
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD
|VC=DIV
|VP=0x050168000000000002100200
|WGT=0
|dbSNPBuildID=137
|rsid=367543070
|GENEINFO=B3GALNT2:148789
|GENE_ID=148789
|GENE_NAME=B3GALNT2
}}{{PMID Auto
|PMID=23453667
|Title=Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of alpha-dystroglycan.
|OA=1
}}