{{Rsnum
|rsid=398124635
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FTL
|position=48965340
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,C,T
|CHROM=19
|CLNACC=RCV000017940.27; RCV000017949.27; RCV000017943.27
|CLNALLE=1; 2; 3
|CLNDBN=Hyperferritinemia cataract syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833213:600886:163
|CLNHGVS=NC_000019.9:g.49468597G>A; NC_000019.9:g.49468597G>C; NC_000019.9:g.49468597G>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0003; 134790.0012; 134790.0006
|Disease=Hyperferritinemia cataract syndrome
|FwdALT=A,C,T
|FwdREF=G
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=G
|RSPOS=49468597
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM;NOV
|VC=SNV
|VP=0x050060000000000002110104
|WGT=0
|dbSNPBuildID=138
|rsid=398124635
}}