{{Rsnum
|rsid=121918361
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ARHGEF9
|position=63724557
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ARHGEF9
}}{{omim
|id=300429
|rsnum=121918361
|variant=0001
}}{{ClinVar
|rsid=121918361
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=62944437
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ARHGEF9:23229
|GENE_NAME=ARHGEF9
|GENE_ID=23229
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.62944437C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300429.0001
|CLNSIG=5
|CLNCUI=C1845102
|CLNDBN=Early infantile epileptic encephalopathy 8
|Disease=Early infantile epileptic encephalopathy 8
|CLNACC=RCV000011796.5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1260:C1845102:300607:163985:2076
}}