{{Rsnum
|rsid=122454126
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=RPS6KA3
|position=20204103
|Gene_s=RPS6KA3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300075
|rsnum=122454126
|variant=0004
}}{{ClinVar
|rsid=122454126
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=20222221
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=RPS6KA3:6197
|GENE_NAME=RPS6KA3
|GENE_ID=6197
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.20222221C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300075.0004
|CLNSIG=5
|CLNCUI=C0265252
|CLNDBN=Coffin-Lowry syndrome
|Disease=Coffin-Lowry syndrome
|CLNACC=RCV000012419.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1346:C0265252:303600:192:15182000
}}