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rs145974360

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs145974360(C;C)
Make rs145974360(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356805
GeneHLA-B
is asnp
is mentioned by
dbSNPrs145974360
ebirs145974360
HLIrs145974360
Exacrs145974360
Varsomers145974360
Maprs145974360
PheGenIrs145974360
hapmaprs145974360
1000 genomesrs145974360
hgdprs145974360
ensemblrs145974360
gopubmedrs145974360
geneviewrs145974360
scholarrs145974360
googlers145974360
pharmgkbrs145974360
gwascentralrs145974360
openSNPrs145974360
23andMers145974360
23andMe allrs145974360
SNP Nexus

SNPshotrs145974360
SNPdbers145974360
MSV3drs145974360
GWAS Ctlgrs145974360
GMAF0.01056
Max Magnitude0
ClinVar
Risk rs145974360(C;C)
Alt rs145974360(C;C)
Reference rs145974360(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324582T>C
CLNSRC
CLNACC