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rs41550015

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41550015(C;T)
Make rs41550015(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356727
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41550015
ebirs41550015
HLIrs41550015
Exacrs41550015
Varsomers41550015
Maprs41550015
PheGenIrs41550015
hapmaprs41550015
1000 genomesrs41550015
hgdprs41550015
ensemblrs41550015
gopubmedrs41550015
geneviewrs41550015
scholarrs41550015
googlers41550015
pharmgkbrs41550015
gwascentralrs41550015
openSNPrs41550015
23andMers41550015
23andMe allrs41550015
SNP Nexus

SNPshotrs41550015
SNPdbers41550015
MSV3drs41550015
GWAS Ctlgrs41550015
Max Magnitude0
ClinVar
Risk rs41550015(T;T)
Alt rs41550015(T;T)
Reference rs41550015(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324504G>A
CLNSRC
CLNACC