{{Rsnum
|rsid = 28937903
|Gene = FKRP
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=A
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Chromosome=19
|position=46756814
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FKRP
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 0.0 | 1.9 | 98.1
| HCB | 0.0 | 1.5 | 98.5
| JPT | 0.0 | 1.8 | 98.2
| YRI | 0.0 | 1.4 | 98.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 1.5 | 98.5
| CHD | 0.0 | 1.9 | 98.1
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.9 | 99.1
| MEX | 1.7 | 1.7 | 96.6
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 1.0 | 99.0
| HapMapRevision=28
}}{{omim
|desc=MUSCULAR DYSTROPHY, CONGENITAL, 1C, WITH NEUROLOGIC ABNORMALITIES
|id=606596
|rsnum=28937903
|variant=0009
}}
{{ neighbor
| rsid = 28937904
| distance = 151
}}

{{ClinVar
|rsid=28937903
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=47260071
|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.47260071C>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;HD;OTHERKG;LSD;OM
|CLNACC=RCV000004447.1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=606596.0009
|Disease=Congenital muscular dystrophy-dystroglycanopathy with mental retardation
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}