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rs41558016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558016(C;C)
Make rs41558016(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356233
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558016
ebirs41558016
HLIrs41558016
Exacrs41558016
Varsomers41558016
Maprs41558016
PheGenIrs41558016
hapmaprs41558016
1000 genomesrs41558016
hgdprs41558016
ensemblrs41558016
gopubmedrs41558016
geneviewrs41558016
scholarrs41558016
googlers41558016
pharmgkbrs41558016
gwascentralrs41558016
openSNPrs41558016
23andMers41558016
23andMe allrs41558016
SNP Nexus

SNPshotrs41558016
SNPdbers41558016
MSV3drs41558016
GWAS Ctlgrs41558016
Max Magnitude0
ClinVar
Risk rs41558016(C,T;C,T)
Alt rs41558016(C,T;C,T)
Reference rs41558016(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324010C>A; NC_000006.11:g.31324010C>G
CLNSRC
CLNACC