{{Rsnum
|rsid=281865071
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=CHRNB2
|position=154571759
|Gene_s=CHRNB2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=1
|CLNACC=RCV000033933.2
|CLNALLE=1
|CLNDBN=Epilepsy, nocturnal frontal lobe, type 3
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1169:C1854335:605375:ORPHA98784
|CLNHGVS=NC_000001.11:g.154571759C>G
|CLNSIG=5
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_000748.2:c.936C>G; NBK1169
|Disease=Epilepsy
|FwdALT=G
|FwdREF=C
|REF=C
|RSPOS=154571759
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD
|VC=SNV
|VP=0x050360000a05000002100100
|WGT=1
|dbSNPBuildID=137
|rsid=281865071
|GENEINFO=CHRNB2:1141
|GENE_ID=1141
|GENE_NAME=CHRNB2
|CLNORIGIN=0
}}