{{Rsnum
|rsid=398124639
|Chromosome=19
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TCTGTC)
|geno3=(TCTGTC;TCTGTC)
|Gene=FTL
|position=48965330
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=19
|CLNACC=RCV000017948.27
|CLNALLE=1
|CLNDBN=Hyperferritinemia cataract syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833213:600886:163
|CLNHGVS=NC_000019.9:g.49468587_49468592delTCTGTC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0011
|Disease=Hyperferritinemia cataract syndrome
|FwdREF=TCTGTC
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=GTCTGTC
|RSPOS=49468586
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=138
|rsid=398124639
}}