{{Rsnum
|rsid=119462986
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=POMT1
|position=131521351
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POMT1
}}{{omim
|id=607423
|rsnum=119462986
|variant=0009
}}{{ClinVar
|rsid=119462986
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=134396738
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=POMT1:10585
|GENE_NAME=POMT1
|GENE_ID=10585
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.134396738G>C
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=14749; 607423.0009
|CLNSIG=5
|CLNCUI=C3150415
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1; not provided
|Disease=Congenital muscular dystrophy-dystroglycanopathy with mental retardation; not provided
|CLNACC=RCV000003402.1; RCV000081485.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3150415:613155
}}