{{Rsnum
|rsid=398122854
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ARX
|position=25015657
|Gene_s=ARX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000022856.6
|CLNALLE=1
|CLNDBN=West syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet:Orphanet:SNOMED_CT
|CLNDSDBID=C0037769:308350:1934:3451:364063:28055006
|CLNHGVS=NC_000023.10:g.25033774G>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300382.0023
|Disease=West syndrome
|FwdALT=G
|FwdREF=C
|GENEINFO=ARX:170302
|GENE_ID=170302
|GENE_NAME=ARX
|REF=G
|RSPOS=25033774
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=138
|rsid=398122854
}}