{{Rsnum
|rsid=119462981
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=POMT1
|position=131510401
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POMT1
}}{{omim
|id=607423
|rsnum=119462981
|variant=0002
}}{{ClinVar
|rsid=119462981
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=134385788
|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.134385788C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000003395.2
|CLNDBN=Walker-Warburg congenital muscular dystrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1291:C0265221:236670:588:899:111504002
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607423.0002
|Disease=Walker-Warburg congenital muscular dystrophy
}}