{{Rsnum
|rsid=104894063
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=CHRNA2
|position=27463607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHRNA2
}}{{omim
|id=118502
|rsnum=104894063
|variant=0001
}}{{ClinVar
|rsid=104894063
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=27321124
|CHROM=8
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050360000000000002110100
|GENEINFO=CHRNA2:1135
|GENE_NAME=CHRNA2
|GENE_ID=1135
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.27321124A>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1169; 118502.0001
|CLNSIG=5
|CLNCUI=C1835905
|CLNDBN=Epilepsy, nocturnal frontal lobe, type 4
|Disease=Epilepsy
|CLNACC=RCV000019056.26
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1169:C1835905:610353:98784
}}