{{Rsnum
|rsid=397509396
|Chromosome=11
|position=66346080
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=B3GNT1
|Gene_s=BRMS1,B3GNT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|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.66113551G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605517.0001
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=66113551
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397509396
|GENEINFO=B3GNT1:11041; BRMS1:25855
|GENE_ID=11041; 25855
|GENE_NAME=B3GNT1; BRMS1
}}