{{Rsnum
|rsid=104894685
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FTL
|position=48966317
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FTL
}}{{omim
|id=134790
|rsnum=104894685
|variant=0013
}}{{ClinVar
|rsid=104894685
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=49469574
|CHROM=19
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FTL:2512
|GENE_NAME=FTL
|GENE_ID=2512
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.49469574G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=134790.0013
|CLNSIG=5
|CLNCUI=C1853578
|CLNDBN=Neuroferritinopathy
|Disease=Neuroferritinopathy
|CLNACC=RCV000017950.22
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1141:C1853578:606159:157846
}}