{{Rsnum
|rsid=121909255
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RAPSN
|position=47447859
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAPSN
}}{{omim
|id=601592
|rsnum=121909255
|variant=0011
}}{{ClinVar
|rsid=121909255
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=47469411
|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.47469411C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601592.0011
|CLNSIG=5
|CLNCUI=C1837091
|CLNDBN=Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
|Disease=Myasthenic syndrome
|CLNACC=RCV000008522.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1168:C1837091:608931:590
}}