{{Rsnum
|rsid=118203993
|Chromosome=12
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ORAI1
|position=121627018
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ORAI1
}}{{omim
|id=610277
|rsnum=118203993
|variant=0001
}}{{ClinVar
|rsid=118203993
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=122064924
|CHROM=12
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ORAI1:84876
|GENE_NAME=ORAI1
|GENE_ID=84876
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.122064924C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610277.0001
|CLNSIG=5
|CLNCUI=C2748568
|CLNDBN=Immune dysfunction with T-cell inactivation due to calcium entry defect 1
|Disease=Immune dysfunction with T-cell inactivation due to calcium entry defect 1
|CLNACC=RCV000001346.2
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2748568:612782:169090:317428
}}