{{Rsnum
|rsid=119463996
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FKTN
|position=105604372
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FKTN
}}{{omim
|id=607440
|rsnum=119463996
|variant=0015
}}{{ClinVar
|rsid=119463996
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=108366653
|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.108366653T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607440.0015
|CLNSIG=5
|CLNCUI=C1969040
|CLNDBN=Limb-girdle muscular dystrophy-dystroglycanopathy, type C4
|Disease=Limb-girdle muscular dystrophy-dystroglycanopathy
|CLNACC=RCV000003358.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1969040:611588:206554
}}