{{Rsnum
|rsid=397514600
|Chromosome=16
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=NOL3
|position=67174230
|Gene_s=NOL3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=16
|CLNACC=RCV000033024.1
|CLNALLE=1
|CLNDBN=Myoclonus, familial cortical
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=CN160752:614937
|CLNHGVS=NC_000016.9:g.67208133G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605235.0001
|Disease=Myoclonus
|FwdALT=C
|FwdREF=G
|GENEINFO=NOL3:8996
|GENE_ID=8996
|GENE_NAME=NOL3
|REF=G
|RSPOS=67208133
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514600
}}