{{Rsnum
|rsid=121909257
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=RAPSN
|position=47442780
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAPSN
}}{{omim
|id=601592
|rsnum=121909257
|variant=0014
}}{{ClinVar
|rsid=121909257
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=47464332
|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.47464332G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601592.0014
|CLNSIG=5
|CLNCUI=C1276035
|CLNDBN=Pena-Shokeir syndrome type I
|Disease=Pena-Shokeir syndrome type I
|CLNACC=RCV000008525.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C1276035:208150:994:401138005
}}