{{Rsnum
|rsid=121909513
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CHRNE
|position=4902311
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CHRNE,C17orf107
}}{{omim
|id=100725
|rsnum=121909513
|variant=0004
}}{{ClinVar
|rsid=121909513
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=4805606
|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.4805606G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=100725.0004
|CLNSIG=5
|CLNCUI=C1837091
|CLNDBN=Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|Disease=Myasthenic syndrome
|CLNACC=RCV000020015.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1168:C1837091:608931:590
}}