{{Rsnum
|rsid = 28935171
|Gene = RPS6KA3
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=X
|position=20155435
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=RPS6KA3
}}{{omim
|desc=COFFIN-LOWRY SYNDROME
|id=300075
|rsnum=28935171
|variant=0009
}}

{{ClinVar
|rsid=28935171
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=20173553
|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.20173553C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300075.0009
|CLNSIG=5
|CLNCUI=C0265252
|CLNDBN=Coffin-Lowry syndrome
|Disease=Coffin-Lowry syndrome
|CLNACC=RCV000012424.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1346:C0265252:303600:192:15182000
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}