{{Rsnum
|rsid=267606814
|Chromosome=9
|position=105617967
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FKTN
|Gene_s=FKTN
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=plus
}}{{ClinVar
|ALT=T
|CHROM=9
|CLNACC=RCV000003371.1
|CLNALLE=1
|CLNDBN=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A4
|CLNHGVS=NC_000009.11:g.108380248C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=607440.0018
|Disease=Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies
|FwdALT=T
|FwdREF=C
|GENEINFO=FKTN:2218
|GENE_ID=2218
|GENE_NAME=FKTN
|REF=C
|RSPOS=108380248
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606814
}}