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rs41558819

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558819(C;T)
Make rs41558819(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356389
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558819
ebirs41558819
HLIrs41558819
Exacrs41558819
Varsomers41558819
Maprs41558819
PheGenIrs41558819
hapmaprs41558819
1000 genomesrs41558819
hgdprs41558819
ensemblrs41558819
gopubmedrs41558819
geneviewrs41558819
scholarrs41558819
googlers41558819
pharmgkbrs41558819
gwascentralrs41558819
openSNPrs41558819
23andMers41558819
23andMe allrs41558819
SNP Nexus

SNPshotrs41558819
SNPdbers41558819
MSV3drs41558819
GWAS Ctlgrs41558819
Max Magnitude0
ClinVar
Risk rs41558819(T;T)
Alt rs41558819(T;T)
Reference rs41558819(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324166G>A
CLNSRC
CLNACC