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rs41559517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559517(-;-)
Make rs41559517(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324029
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559517
ebirs41559517
HLIrs41559517
Exacrs41559517
Varsomers41559517
Maprs41559517
PheGenIrs41559517
hapmaprs41559517
1000 genomesrs41559517
hgdprs41559517
ensemblrs41559517
gopubmedrs41559517
geneviewrs41559517
scholarrs41559517
googlers41559517
pharmgkbrs41559517
gwascentralrs41559517
openSNPrs41559517
23andMers41559517
23andMe allrs41559517
SNP Nexus

SNPshotrs41559517
SNPdbers41559517
MSV3drs41559517
GWAS Ctlgrs41559517
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41559517(;)
Alt rs41559517(;)
Reference rs41559517(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324029delC
CLNSRC
CLNACC