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rs41548113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41548113(A;G)
Make rs41548113(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356744
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41548113
ebirs41548113
HLIrs41548113
Exacrs41548113
Varsomers41548113
Maprs41548113
PheGenIrs41548113
hapmaprs41548113
1000 genomesrs41548113
hgdprs41548113
ensemblrs41548113
gopubmedrs41548113
geneviewrs41548113
scholarrs41548113
googlers41548113
pharmgkbrs41548113
gwascentralrs41548113
openSNPrs41548113
23andMers41548113
23andMe allrs41548113
SNP Nexus

SNPshotrs41548113
SNPdbers41548113
MSV3drs41548113
GWAS Ctlgrs41548113
Max Magnitude0
ClinVar
Risk rs41548113(G,T;G,T)
Alt rs41548113(G,T;G,T)
Reference rs41548113(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324521T>A; NC_000006.11:g.31324521T>C
CLNSRC
CLNACC