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rs41558013

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558013(A;A)
Make rs41558013(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356788
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558013
ebirs41558013
HLIrs41558013
Exacrs41558013
Varsomers41558013
Maprs41558013
PheGenIrs41558013
hapmaprs41558013
1000 genomesrs41558013
hgdprs41558013
ensemblrs41558013
gopubmedrs41558013
geneviewrs41558013
scholarrs41558013
googlers41558013
pharmgkbrs41558013
gwascentralrs41558013
openSNPrs41558013
23andMers41558013
23andMe allrs41558013
SNP Nexus

SNPshotrs41558013
SNPdbers41558013
MSV3drs41558013
GWAS Ctlgrs41558013
Max Magnitude0
ClinVar
Risk rs41558013(A,C,T;A,C,T)
Alt rs41558013(A,C,T;A,C,T)
Reference rs41558013(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324565C>A; NC_000006.11:g.31324565C>G; NC_000006.11:g.31324565C>T
CLNSRC
CLNACC