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rs41558318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41558318(A;G)
Make rs41558318(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355384
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558318
ebirs41558318
HLIrs41558318
Exacrs41558318
Varsomers41558318
Maprs41558318
PheGenIrs41558318
hapmaprs41558318
1000 genomesrs41558318
hgdprs41558318
ensemblrs41558318
gopubmedrs41558318
geneviewrs41558318
scholarrs41558318
googlers41558318
pharmgkbrs41558318
gwascentralrs41558318
openSNPrs41558318
23andMers41558318
23andMe allrs41558318
SNP Nexus

SNPshotrs41558318
SNPdbers41558318
MSV3drs41558318
GWAS Ctlgrs41558318
Max Magnitude0
ClinVar
Risk rs41558318(G;G)
Alt rs41558318(G;G)
Reference rs41558318(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323161T>C
CLNSRC
CLNACC