{{Rsnum
|rsid=398124638
|Chromosome=19
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FTL
|position=48965359
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000017946.27
|CLNALLE=1
|CLNDBN=Hyperferritinemia cataract syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833213:600886:163
|CLNHGVS=NC_000019.9:g.49468616G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0009
|Disease=Hyperferritinemia cataract syndrome
|FwdALT=C
|FwdREF=G
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=G
|RSPOS=49468616
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398124638
}}