{{Rsnum
|rsid=45439799
|Gene=ATRX
|Chromosome=X
|position=77600552
|Orientation=minus
|GMAF=0.003628
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ATRX
}}{{omim
|id=300032
|rsnum=45439799
|variant=0004
}}{{ClinVar
|rsid=45439799
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=76856021
|CHROM=X
|GMAF=0.00361664
|dbSNPBuildID=127
|SSR=0
|SAO=1
|VP=0x050060000000050516110100
|GENEINFO=ATRX:546
|GENE_NAME=ATRX
|GENE_ID=546
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.76856021T>C
|CLNSRC=Emory University; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=9908; 300032.0004
|CLNSIG=5
|CLNCUI=C1845055
|CLNDBN=ATR-X syndrome; AllHighlyPenetrant
|Disease=ATR-X syndrome; AllHighlyPenetrant
|CLNACC=RCV000012490.15; RCV000078966.1
|Tags=RV;PM;VLD;G5;HD;GNO;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9964; 0.003628
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1449:C1845055:301040:847; CN169374
|COMMON=1
}}