{{Rsnum
|rsid=397515390
|Chromosome=11
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=STIM1
|position=4082183
|Gene_s=STIM1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=11
|CLNACC=RCV000023497.3
|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.4103413G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605921.0002
|Disease=Immune dysfunction with T-cell inactivation due to calcium entry defect 2
|FwdALT=A
|FwdREF=G
|GENEINFO=STIM1:6786
|GENE_ID=6786
|GENE_NAME=STIM1
|REF=G
|RSPOS=4103413
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397515390
}}