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rs878853261

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853261(-;-)
Make rs878853261(-;A)
Make rs878853261(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position121627008
GeneORAI1
is asnp
is mentioned by
dbSNPrs878853261
ebirs878853261
HLIrs878853261
Exacrs878853261
Varsomers878853261
Maprs878853261
PheGenIrs878853261
hapmaprs878853261
1000 genomesrs878853261
hgdprs878853261
ensemblrs878853261
gopubmedrs878853261
geneviewrs878853261
scholarrs878853261
googlers878853261
pharmgkbrs878853261
gwascentralrs878853261
openSNPrs878853261
23andMers878853261
23andMe allrs878853261
SNP Nexus

SNPshotrs878853261
SNPdbers878853261
MSV3drs878853261
GWAS Ctlgrs878853261
Max Magnitude0
ClinVar
Risk rs878853261(A;A)
Alt rs878853261(A;A)
Reference rs878853261(;)
Significance Pathogenic
Disease Immune dysfunction with T-cell inactivation due to calcium entry defect 1
Variation info
Gene ORAI1
CLNDBN Immune dysfunction with T-cell inactivation due to calcium entry defect 1
Reversed 0
HGVS NC_000012.11:g.122064914dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000172858.2,