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rs41545913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545913(-;-)
Make rs41545913(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324034
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545913
ebirs41545913
HLIrs41545913
Exacrs41545913
Varsomers41545913
Maprs41545913
PheGenIrs41545913
hapmaprs41545913
1000 genomesrs41545913
hgdprs41545913
ensemblrs41545913
gopubmedrs41545913
geneviewrs41545913
scholarrs41545913
googlers41545913
pharmgkbrs41545913
gwascentralrs41545913
openSNPrs41545913
23andMers41545913
23andMe allrs41545913
SNP Nexus

SNPshotrs41545913
SNPdbers41545913
MSV3drs41545913
GWAS Ctlgrs41545913
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41545913(;)
Alt rs41545913(;)
Reference rs41545913(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324034delC
CLNSRC
CLNACC