{{Rsnum
|rsid=398124637
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=FTL
|position=48965344
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=19
|CLNACC=RCV000017945.27; RCV000082859.1
|CLNALLE=1; 2
|CLNDBN=Hyperferritinemia cataract syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833213:600886:163
|CLNHGVS=NC_000019.9:g.49468601C>A; NC_000019.9:g.49468601C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0008; 134790.0020
|Disease=Hyperferritinemia cataract syndrome
|FwdALT=A,T
|FwdREF=C
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=C
|RSPOS=49468601
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398124637
}}