{{Rsnum
|rsid=199422328
|Chromosome=20
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=ADA
|position=44626597
|Gene_s=ADA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199422328
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=43255238
|CHROM=20
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.43255238C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=608958.0025
|CLNSIG=5
|CLNCUI=C1863236
|CLNDBN=Severe combined immunodeficiency due to ADA deficiency
|Disease=Severe combined immunodeficiency due to ADA deficiency
|CLNACC=RCV000002054.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1483:C1863236:102700:277
|GENEINFO=ADA:100
|GENE_ID=100
|GENE_NAME=ADA
}}