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rs41546113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41546113(C;T)
Make rs41546113(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356240
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546113
ebirs41546113
HLIrs41546113
Exacrs41546113
Varsomers41546113
Maprs41546113
PheGenIrs41546113
hapmaprs41546113
1000 genomesrs41546113
hgdprs41546113
ensemblrs41546113
gopubmedrs41546113
geneviewrs41546113
scholarrs41546113
googlers41546113
pharmgkbrs41546113
gwascentralrs41546113
openSNPrs41546113
23andMers41546113
23andMe allrs41546113
SNP Nexus

SNPshotrs41546113
SNPdbers41546113
MSV3drs41546113
GWAS Ctlgrs41546113
Max Magnitude0
ClinVar
Risk rs41546113(T;T)
Alt rs41546113(T;T)
Reference rs41546113(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324017G>A
CLNSRC
CLNACC