{{Rsnum
|rsid=119463992
|Chromosome=9
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FKTN
|position=105617968
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FKTN
}}{{omim
|id=607440
|rsnum=119463992
|variant=0009
}}{{ClinVar
|rsid=119463992
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=108380249
|CHROM=9
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FKTN:2218
|GENE_NAME=FKTN
|GENE_ID=2218
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000009.11:g.108380249G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607440.0009
|CLNSIG=5
|CLNCUI=C1969040; C2751052
|CLNDBN=Limb-girdle muscular dystrophy-dystroglycanopathy, type C4; Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B4
|Disease=Limb-girdle muscular dystrophy-dystroglycanopathy; Congenital muscular dystrophy-dystroglycanopathy without mental retardation
|CLNACC=RCV000003362.2; RCV000003363.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM
|CLNDSDBID=C1969040:611588:206554; NBK1291:C2751052:613152
}}