{{Rsnum
|rsid=122461160
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=IL1RAPL1
|position=29955106
|Gene_s=IL1RAPL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300206
|variant=0001
|rsnum=122461160
}}{{ClinVar
|rsid=122461160
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=29973223
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=IL1RAPL1:11141
|GENE_NAME=IL1RAPL1
|GENE_ID=11141
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.29973223C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300206.0001
|CLNSIG=5
|CLNCUI=C0796227
|CLNDBN=X-linked mental retardation 21
|Disease=X-linked mental retardation 21
|CLNACC=RCV000012235.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C0796227:300143:777
}}