{{Rsnum
|rsid=122445102
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATRX
|position=77633210
|Gene_s=ATRX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300032
|rsnum=122445102
|variant=0012
}}{{ClinVar
|rsid=122445102
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=76888698
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ATRX:546
|GENE_NAME=ATRX
|GENE_ID=546
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.76888698G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000012498.23
|CLNDBN=MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300032.0012
|Disease=MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME
}}