{{Rsnum
|rsid=121909118
|Chromosome=4
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=SCARB2
|position=76174276
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SCARB2
}}{{omim
|id=602257
|rsnum=121909118
|variant=0003
}}{{ClinVar
|rsid=121909118
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=77095429
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=SCARB2:950
|GENE_NAME=SCARB2
|GENE_ID=950
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.77095429G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602257.0003
|CLNSIG=5
|CLNCUI=C0751779
|CLNDBN=Epilepsy, progressive myoclonic 4, with or without renal failure
|Disease=Epilepsy
|CLNACC=RCV000007803.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0751779:254900:163696
}}