Have questions? Visit https://www.reddit.com/r/SNPedia

rs41541124

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41541124(C;C)
Make rs41541124(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356033
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41541124
ebirs41541124
HLIrs41541124
Exacrs41541124
Varsomers41541124
Maprs41541124
PheGenIrs41541124
hapmaprs41541124
1000 genomesrs41541124
hgdprs41541124
ensemblrs41541124
gopubmedrs41541124
geneviewrs41541124
scholarrs41541124
googlers41541124
pharmgkbrs41541124
gwascentralrs41541124
openSNPrs41541124
23andMers41541124
23andMe allrs41541124
SNP Nexus

SNPshotrs41541124
SNPdbers41541124
MSV3drs41541124
GWAS Ctlgrs41541124
GMAF0.01974
Max Magnitude0
ClinVar
Risk rs41541124(C;C)
Alt rs41541124(C;C)
Reference rs41541124(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323810A>G
CLNSRC
CLNACC