{{Rsnum
|rsid=397514671
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=STIM1
|position=4083309
|Gene_s=STIM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000034350.3
|CLNALLE=1
|CLNDBN=Immune dysfunction with T-cell inactivation due to calcium entry defect 2
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C2748557:612783:169090:317430
|CLNHGVS=NC_000011.9:g.4104539C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605921.0003
|Disease=Immune dysfunction with T-cell inactivation due to calcium entry defect 2
|FwdALT=T
|FwdREF=C
|GENEINFO=STIM1:6786
|GENE_ID=6786
|GENE_NAME=STIM1
|REF=C
|RSPOS=4104539
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514671
}}