{{Rsnum
|rsid=80338740
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TTC)
|geno3=(TTC;TTC)
|Gene=SLC6A8
|position=153693985
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=SLC6A8
}}{{omim
|id=300036
|rsnum=80338740
|variant=0003
}}{{ClinVar
|rsid=80338740
|Reversed=0
|FwdREF=TTC
|FwdALT=
|REF=GTTC
|ALT=G
|RSPOS=152959433
|CHROM=X
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=SLC6A8:6535
|GENE_NAME=SLC6A8
|GENE_ID=6535
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.152959440_152959442delTTC
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK3794; 300036.0003
|CLNSIG=5
|CLNCUI=C1845862; C1845862
|CLNDBN=Creatine deficiency, X-linked
|Disease=Creatine deficiency
|CLNACC=RCV000012464.16
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK3794:C1845862:300352:52503
}}{{PMID|12210795}} X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8.