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rs41558918

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558918(G;T)
Make rs41558918(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356997
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558918
ebirs41558918
HLIrs41558918
Exacrs41558918
Varsomers41558918
Maprs41558918
PheGenIrs41558918
hapmaprs41558918
1000 genomesrs41558918
hgdprs41558918
ensemblrs41558918
gopubmedrs41558918
geneviewrs41558918
scholarrs41558918
googlers41558918
pharmgkbrs41558918
gwascentralrs41558918
openSNPrs41558918
23andMers41558918
23andMe allrs41558918
SNP Nexus

SNPshotrs41558918
SNPdbers41558918
MSV3drs41558918
GWAS Ctlgrs41558918
Max Magnitude0
ClinVar
Risk rs41558918(T;T)
Alt rs41558918(T;T)
Reference rs41558918(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324774C>A
CLNSRC
CLNACC