{{Rsnum
|rsid = 28999110
|Gene = CHRNE
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=17
|position=4901071
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHRNE,C17orf107
}}{{omim
|desc=MYASTHENIC SYNDROME, SLOW-CHANNEL CONGENITAL
|id=100725
|rsnum=28999110
|variant=0010
}}

{{ClinVar
|rsid=28999110
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=4804366
|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.4804366G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=100725.0010
|CLNSIG=5
|CLNCUI=C0751885
|CLNDBN=Myasthenic syndrome, slow-channel congenital
|Disease=Myasthenic syndrome
|CLNACC=RCV000020020.25
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1168:C0751885:601462:590
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}