{{Rsnum
|rsid=121908718
|Chromosome=20
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=ADA
|position=44621103
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ADA
}}{{omim
|id=608958
|rsnum=121908718
|variant=0009
}}{{ClinVar
|rsid=121908718
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=43249744
|CHROM=20
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ADA:100
|GENE_NAME=ADA
|GENE_ID=100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000020.10:g.43249744G>T
|CLNORIGIN=0
|CLNSIG=5
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNACC=RCV000002038.1; RCV000059115.1
|CLNDBN=Partial adenosine deaminase deficiency; Severe combined immunodeficiency due to ADA deficiency
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=C1863239; NBK1483:C1863236:102700:277
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNSRCID=608958.0009; VAR_002238
|Disease=Partial adenosine deaminase deficiency; Severe combined immunodeficiency due to ADA deficiency
}}{{PMID Auto
|PMID=2783588
|Title=Identification of a point mutation resulting in a heat-labile adenosine deaminase (ADA) in two unrelated children with partial ADA deficiency.
|OA=1
}}