{{Rsnum
|rsid=119462987
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=POMT1
|position=131522160
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POMT1
}}{{omim
|id=607423
|rsnum=119462987
|variant=0013
}}{{ClinVar
|rsid=119462987
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=134397547
|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.134397547G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607423.0013
|CLNSIG=5
|CLNCUI=C3150415
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1
|Disease=Congenital muscular dystrophy-dystroglycanopathy with mental retardation
|CLNACC=RCV000003406.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C3150415:613155
}}