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rs41545013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41545013(G;G)
Make rs41545013(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354914
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545013
ebirs41545013
HLIrs41545013
Exacrs41545013
Varsomers41545013
Maprs41545013
PheGenIrs41545013
hapmaprs41545013
1000 genomesrs41545013
hgdprs41545013
ensemblrs41545013
gopubmedrs41545013
geneviewrs41545013
scholarrs41545013
googlers41545013
pharmgkbrs41545013
gwascentralrs41545013
openSNPrs41545013
23andMers41545013
23andMe allrs41545013
SNP Nexus

SNPshotrs41545013
SNPdbers41545013
MSV3drs41545013
GWAS Ctlgrs41545013
Max Magnitude0
ClinVar
Risk rs41545013(G;G)
Alt rs41545013(G;G)
Reference rs41545013(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322691A>C
CLNSRC
CLNACC