{{Rsnum
|rsid=199422235
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KDM5C
|position=53211867
|Gene_s=KDM5C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199422235
|Reversed=1
|FwdREF=G
|FwdALT=C
|REF=C
|ALT=G
|RSPOS=53241049
|CHROM=X
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.53241049C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=314690.0003
|CLNSIG=5
|CLNCUI=C1845243
|CLNDBN=X-linked mental retardation, syndromic, Claes-Jensen type
|Disease=X-linked mental retardation
|CLNACC=RCV000010428.3
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845243:300534:85279
|GENEINFO=KDM5C:8242
|GENE_ID=8242
|GENE_NAME=KDM5C
}}