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rs863223293

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223293(A;A)
Make rs863223293(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position10907555
GeneCIITA
is asnp
is mentioned by
dbSNPrs863223293
ebirs863223293
HLIrs863223293
Exacrs863223293
Varsomers863223293
Maprs863223293
PheGenIrs863223293
hapmaprs863223293
1000 genomesrs863223293
hgdprs863223293
ensemblrs863223293
gopubmedrs863223293
geneviewrs863223293
scholarrs863223293
googlers863223293
pharmgkbrs863223293
gwascentralrs863223293
openSNPrs863223293
23andMers863223293
23andMe allrs863223293
SNP Nexus

SNPshotrs863223293
SNPdbers863223293
MSV3drs863223293
GWAS Ctlgrs863223293
Max Magnitude0
ClinVar
Risk rs863223293(A;A)
Alt rs863223293(A;A)
Reference rs863223293(G;G)
Significance Pathogenic
Disease Bare lymphocyte syndrome type 2
Variation info
Gene CIITA
CLNDBN Bare lymphocyte syndrome type 2, complementation group A
Reversed 0
HGVS NC_000016.9:g.11001412G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010151.3,