{{Rsnum
|rsid=387906267
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ADA
|position=44626601
|Gene_s=ADA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=20
|CLNACC=RCV000002046.1
|CLNALLE=1
|CLNDBN=Severe combined immunodeficiency due to ADA deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1483:C1863236:102700:277
|CLNHGVS=NC_000020.10:g.43255242T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608958.0017
|Disease=Severe combined immunodeficiency due to ADA deficiency
|FwdALT=G
|FwdREF=A
|REF=T
|RSPOS=43255242
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906267
|GENEINFO=ADA:100
|GENE_ID=100
|GENE_NAME=ADA
}}