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rs41558815

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41558815(C;T)
Make rs41558815(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position31356973
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558815
ebirs41558815
HLIrs41558815
Exacrs41558815
Varsomers41558815
Maprs41558815
PheGenIrs41558815
hapmaprs41558815
1000 genomesrs41558815
hgdprs41558815
ensemblrs41558815
gopubmedrs41558815
geneviewrs41558815
scholarrs41558815
googlers41558815
pharmgkbrs41558815
gwascentralrs41558815
openSNPrs41558815
23andMers41558815
23andMe allrs41558815
SNP Nexus

SNPshotrs41558815
SNPdbers41558815
MSV3drs41558815
GWAS Ctlgrs41558815
GMAF0.05693
Max Magnitude0
ClinVar
Risk rs41558815(T;T)
Alt rs41558815(T;T)
Reference rs41558815(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324750G>A
CLNSRC
CLNACC