{{Rsnum
|rsid=104894300
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAPSN
|position=47448924
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAPSN
}}{{omim
|id=601592
|rsnum=104894300
|variant=0002
}}{{ClinVar
|rsid=104894300
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=47470476
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RAPSN:5913
|GENE_NAME=RAPSN
|GENE_ID=5913
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.47470476A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601592.0002
|CLNSIG=5
|CLNCUI=C1837091
|CLNDBN=Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|Disease=Myasthenic syndrome
|CLNACC=RCV000008513.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1168:C1837091:608931:590
}}