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rs41545339

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545339(C;T)
Make rs41545339(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355930
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545339
ebirs41545339
HLIrs41545339
Exacrs41545339
Varsomers41545339
Maprs41545339
PheGenIrs41545339
hapmaprs41545339
1000 genomesrs41545339
hgdprs41545339
ensemblrs41545339
gopubmedrs41545339
geneviewrs41545339
scholarrs41545339
googlers41545339
pharmgkbrs41545339
gwascentralrs41545339
openSNPrs41545339
23andMers41545339
23andMe allrs41545339
SNP Nexus

SNPshotrs41545339
SNPdbers41545339
MSV3drs41545339
GWAS Ctlgrs41545339
GMAF0.03306
Max Magnitude0
ClinVar
Risk rs41545339(T;T)
Alt rs41545339(T;T)
Reference rs41545339(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323707G>A
CLNSRC
CLNACC