{{Rsnum
|rsid=398124636
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FTL
|position=48965347
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=19
|CLNACC=RCV000017944.24
|CLNALLE=1
|CLNDBN=Hyperferritinemia cataract syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833213:600886:163
|CLNHGVS=NC_000019.9:g.49468604C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0007
|Disease=Hyperferritinemia cataract syndrome
|FwdALT=T
|FwdREF=C
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=C
|RSPOS=49468604
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398124636
}}