{{Rsnum
|rsid=122445111
|Chromosome=X
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATRX
|position=77684942
|Gene_s=ATRX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300032
|rsnum=122445111
|variant=0025
}}{{ClinVar
|rsid=122445111
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=76940434
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ATRX:546
|GENE_NAME=ATRX
|GENE_ID=546
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.76940434C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000012511.13
|CLNDBN=MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300032.0025
|Disease=MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME
}}