{{Rsnum
|rsid=397509397
|Chromosome=11
|position=66346129
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=B3GNT1
|Gene_s=BRMS1,B3GNT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=11
|CLNACC=RCV000043695.2
|CLNALLE=1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A13
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN177021:615287:899
|CLNHGVS=NC_000011.9:g.66113600T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605517.0001
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=66113600
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397509397
|GENEINFO=B3GNT1:11041; BRMS1:25855
|GENE_ID=11041; 25855
|GENE_NAME=B3GNT1; BRMS1
}}