{{Rsnum
|rsid=118203977
|Chromosome=4
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MFSD8
|position=127930787
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MFSD8
}}{{omim
|id=611124
|rsnum=118203977
|variant=0003
}}{{ClinVar
|rsid=118203977
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=128851942
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=MFSD8:256471
|GENE_NAME=MFSD8
|GENE_ID=256471
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.128851942A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=611124.0003
|CLNSIG=5
|CLNCUI=C1838571
|CLNDBN=Ceroid lipofuscinosis neuronal 7
|Disease=Ceroid lipofuscinosis neuronal 7
|CLNACC=RCV000001058.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1838571:610951:168491:228366
}}