{{Rsnum
|rsid=139732572
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FTL
|position=48965508
|Gene_s=FTL
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=19
|CLNACC=RCV000082857.1
|CLNALLE=1
|CLNDBN=L-FERRITIN DEFICIENCY
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN183734:615604
|CLNHGVS=NC_000019.9:g.49468765A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=134790.0018
|Disease=L-FERRITIN DEFICIENCY
|FwdALT=G
|FwdREF=A
|GENEINFO=FTL:2512
|GENE_ID=2512
|GENE_NAME=FTL
|REF=A
|RSPOS=49468765
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=139732572
}}