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rs137852602

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852602(G;T)
Make rs137852602(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position10906633
GeneCIITA
is asnp
is mentioned by
dbSNPrs137852602
ebirs137852602
HLIrs137852602
Exacrs137852602
Varsomers137852602
Maprs137852602
PheGenIrs137852602
hapmaprs137852602
1000 genomesrs137852602
hgdprs137852602
ensemblrs137852602
gopubmedrs137852602
geneviewrs137852602
scholarrs137852602
googlers137852602
pharmgkbrs137852602
gwascentralrs137852602
openSNPrs137852602
23andMers137852602
23andMe allrs137852602
SNP Nexus

SNPshotrs137852602
SNPdbers137852602
MSV3drs137852602
GWAS Ctlgrs137852602
Max Magnitude0
OMIM600005
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137852602(T;T)
Alt rs137852602(T;T)
Reference rs137852602(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.11000490G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010149.6,