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rs41545517

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545517(C;T)
Make rs41545517(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355391
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545517
ebirs41545517
HLIrs41545517
Exacrs41545517
Varsomers41545517
Maprs41545517
PheGenIrs41545517
hapmaprs41545517
1000 genomesrs41545517
hgdprs41545517
ensemblrs41545517
gopubmedrs41545517
geneviewrs41545517
scholarrs41545517
googlers41545517
pharmgkbrs41545517
gwascentralrs41545517
openSNPrs41545517
23andMers41545517
23andMe allrs41545517
SNP Nexus

SNPshotrs41545517
SNPdbers41545517
MSV3drs41545517
GWAS Ctlgrs41545517
Max Magnitude0
ClinVar
Risk rs41545517(T;T)
Alt rs41545517(T;T)
Reference rs41545517(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323168G>A
CLNSRC
CLNACC