{{Rsnum
|rsid = 28937902
|Gene = FKRP
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=19
|position=46756113
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FKRP
}}{{omim
|desc=MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES
|id=606596
|rsnum=28937902
|variant=0008
}}
{{ neighbor
| rsid = 28937905
| distance = 503
}}
{{ neighbor
| rsid = 28937900
| distance = 163
}}

{{ClinVar
|rsid=28937902
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=47259370
|CHROM=19
|dbSNPBuildID=129
|SSR=0
|SAO=1
|VP=0x050060000000000402110100
|GENEINFO=FKRP:79147
|GENE_NAME=FKRP
|GENE_ID=79147
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.47259370C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;HD;OTHERKG;LSD;OM
|CLNACC=RCV000004446.1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606596.0008
|Disease=Congenital muscular dystrophy-dystroglycanopathy with mental retardation
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}