{{Rsnum
|rsid = 28941782
|Gene = POMT1
|Orientation=plus
|ReferenceAllele=G
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Chromosome=9
|position=131506217
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=POMT1
}}{{omim
|desc=WALKER-WARBURG SYNDROME
|id=607423
|rsnum=28941782
|variant=0001
}}

{{ClinVar
|rsid=28941782
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=134381604
|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.134381604G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000003394.2
|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=607423.0001
|Disease=Walker-Warburg congenital muscular dystrophy
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}