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rs45611338

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs45611338(-;-)
Make rs45611338(-;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355895
GeneHLA-B
is asnp
is mentioned by
dbSNPrs45611338
ebirs45611338
HLIrs45611338
Exacrs45611338
Varsomers45611338
Maprs45611338
PheGenIrs45611338
hapmaprs45611338
1000 genomesrs45611338
hgdprs45611338
ensemblrs45611338
gopubmedrs45611338
geneviewrs45611338
scholarrs45611338
googlers45611338
pharmgkbrs45611338
gwascentralrs45611338
openSNPrs45611338
23andMers45611338
23andMe allrs45611338
SNP Nexus

SNPshotrs45611338
SNPdbers45611338
MSV3drs45611338
GWAS Ctlgrs45611338
GMAF0.01745
Max Magnitude0
ClinVar
Risk rs45611338(;)
Alt rs45611338(;)
Reference rs45611338(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323672delA
CLNSRC
CLNACC