{{Rsnum
|rsid=387906268
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ADA
|position=44619862
|Gene_s=ADA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=20
|CLNACC=RCV000002059.1
|CLNALLE=1
|CLNDBN=SCID due to ADA deficiency, delayed onset
|CLNDSDB=MedGen
|CLNDSDBID=C1863237
|CLNHGVS=NC_000020.10:g.43248503A>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608958.0030
|Disease=SCID due to ADA deficiency
|FwdALT=A
|FwdREF=T
|REF=A
|RSPOS=43248503
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906268
|GENEINFO=ADA:100
|GENE_ID=100
|GENE_NAME=ADA
}}