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rs41559921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41559921(C;G)
Make rs41559921(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356926
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559921
ebirs41559921
HLIrs41559921
Exacrs41559921
Varsomers41559921
Maprs41559921
PheGenIrs41559921
hapmaprs41559921
1000 genomesrs41559921
hgdprs41559921
ensemblrs41559921
gopubmedrs41559921
geneviewrs41559921
scholarrs41559921
googlers41559921
pharmgkbrs41559921
gwascentralrs41559921
openSNPrs41559921
23andMers41559921
23andMe allrs41559921
SNP Nexus

SNPshotrs41559921
SNPdbers41559921
MSV3drs41559921
GWAS Ctlgrs41559921
GMAF0.03398
Max Magnitude0
ClinVar
Risk rs41559921(G,T;G,T)
Alt rs41559921(G,T;G,T)
Reference rs41559921(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324703G>A; NC_000006.11:g.31324703G>C
CLNSRC
CLNACC