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rs41559422

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559422(C;T)
Make rs41559422(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355890
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559422
ebirs41559422
HLIrs41559422
Exacrs41559422
Varsomers41559422
Maprs41559422
PheGenIrs41559422
hapmaprs41559422
1000 genomesrs41559422
hgdprs41559422
ensemblrs41559422
gopubmedrs41559422
geneviewrs41559422
scholarrs41559422
googlers41559422
pharmgkbrs41559422
gwascentralrs41559422
openSNPrs41559422
23andMers41559422
23andMe allrs41559422
SNP Nexus

SNPshotrs41559422
SNPdbers41559422
MSV3drs41559422
GWAS Ctlgrs41559422
GMAF0.02479
Max Magnitude0
ClinVar
Risk rs41559422(T;T)
Alt rs41559422(T;T)
Reference rs41559422(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323667G>A
CLNSRC
CLNACC