{{Rsnum
|rsid=122445106
|Chromosome=X
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ATRX
|position=77633660
|Gene_s=ATRX
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300032
|rsnum=122445106
|variant=0019
}}{{ClinVar
|rsid=122445106
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=76889148
|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.76889148G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300032.0019
|CLNSIG=5
|CLNCUI=C1845055
|CLNDBN=ATR-X syndrome
|Disease=ATR-X syndrome
|CLNACC=RCV000012505.23
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1449:C1845055:301040:847
}}