{{Rsnum
|rsid=121909511
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CHRNE
|position=4900845
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHRNE,C17orf107
}}{{omim
|id=100725
|rsnum=121909511
|variant=0002
}}{{ClinVar
|rsid=121909511
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=4804140
|CHROM=17
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=C17orf107:100130311; CHRNE:1145
|GENE_NAME=C17orf107; CHRNE
|GENE_ID=100130311; 1145
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.4804140G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=100725.0002
|CLNSIG=5
|CLNCUI=C0751885
|CLNDBN=Myasthenic syndrome, slow-channel congenital
|Disease=Myasthenic syndrome
|CLNACC=RCV000020012.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1168:C0751885:601462:590
}}