{{Rsnum
|rsid=398124640
|Chromosome=19
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GGCCCGGAGGCTGGGC)
|geno3=(GGCCCGGAGGCTGGGC;GGCCCGGAGGCTGGGC)
|Gene=FTL
|position=48966691
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TGGCCCGGAGGCTGGGC
|CHROM=19
|CLNACC=RCV000017952.23
|CLNALLE=1
|CLNDBN=Neuroferritinopathy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1141:C1853578:606159:157846
|CLNHGVS=NC_000019.9:g.49469933_49469948dup16
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0015
|Disease=Neuroferritinopathy
|FwdALT=GGCCCGGAGGCTGGGC
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=T
|RSPOS=49469932
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398124640
}}