{{Rsnum
|rsid=137852859
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=NHLRC1
|position=18121684
|Gene_s=NHLRC1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608072
|variant=0007
|rsnum=137852859
}}{{ClinVar
|rsid=137852859
|Reversed=1
|FwdREF=A
|FwdALT=C
|REF=T
|ALT=G
|RSPOS=18121915
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=NHLRC1:378884
|GENE_NAME=NHLRC1
|GENE_ID=378884
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.18121915T>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000002710.2
|CLNDBN=Epilepsy, progressive myoclonic 2b
|CLNDSDB=MedGen
|CLNDSDBID=C1850764
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608072.0007
|Disease=Epilepsy
}}