{{Rsnum
|rsid=104894634
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=RAI1
|position=17797633
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RAI1
}}{{omim
|id=607642
|rsnum=104894634
|variant=0005
}}{{ClinVar
|rsid=104894634
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=17700947
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=RAI1:10743
|GENE_NAME=RAI1
|GENE_ID=10743
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.17700947A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=607642.0005
|CLNSIG=5
|CLNCUI=C0795864
|CLNDBN=Smith-Magenis syndrome
|Disease=Smith-Magenis syndrome
|CLNACC=RCV000003084.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1310:C0795864:182290:819:401315004
}}