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rs771073292

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs771073292(A;A)
Make rs771073292(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position10922491
GeneCIITA
is asnp
is mentioned by
dbSNPrs771073292
ebirs771073292
HLIrs771073292
Exacrs771073292
Varsomers771073292
Maprs771073292
PheGenIrs771073292
hapmaprs771073292
1000 genomesrs771073292
hgdprs771073292
ensemblrs771073292
gopubmedrs771073292
geneviewrs771073292
scholarrs771073292
googlers771073292
pharmgkbrs771073292
gwascentralrs771073292
openSNPrs771073292
23andMers771073292
23andMe allrs771073292
SNP Nexus

SNPshotrs771073292
SNPdbers771073292
MSV3drs771073292
GWAS Ctlgrs771073292
Max Magnitude0
ClinVar
Risk rs771073292(A;A)
Alt rs771073292(A;A)
Reference rs771073292(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.11016348G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010150.4,