{{Rsnum
|rsid=119463991
|Chromosome=9
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FKTN
|position=105601325
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FKTN
}}{{omim
|id=607440
|rsnum=119463991
|variant=0007
}}{{ClinVar
|rsid=119463991
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=108363606
|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.108363606C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000003360.1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A4
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607440.0007
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
}}