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rs41545616

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41545616(C;C)
Make rs41545616(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355154
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545616
ebirs41545616
HLIrs41545616
Exacrs41545616
Varsomers41545616
Maprs41545616
PheGenIrs41545616
hapmaprs41545616
1000 genomesrs41545616
hgdprs41545616
ensemblrs41545616
gopubmedrs41545616
geneviewrs41545616
scholarrs41545616
googlers41545616
pharmgkbrs41545616
gwascentralrs41545616
openSNPrs41545616
23andMers41545616
23andMe allrs41545616
SNP Nexus

SNPshotrs41545616
SNPdbers41545616
MSV3drs41545616
GWAS Ctlgrs41545616
Max Magnitude0
ClinVar
Risk rs41545616(C;C)
Alt rs41545616(C;C)
Reference rs41545616(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322931A>G
CLNSRC
CLNACC