{{Rsnum
|rsid=137852222
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=MAGT1
|position=77841311
|Gene_s=MAGT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300715
|variant=0001
|rsnum=137852222
}}{{ClinVar
|rsid=137852222
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=77096808
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000a01000002110100
|GENEINFO=MAGT1:84061
|GENE_NAME=MAGT1
|GENE_ID=84061
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.77096808A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300715.0001
|CLNSIG=5
|CLNCUI=C2678034
|CLNDBN=X-linked mental retardation 95
|Disease=X-linked mental retardation 95
|CLNACC=RCV000011416.1
|Tags=RV;PM;NSM;REF;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2678034:300716:777
}}