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rs41552112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41552112(A;T)
Make rs41552112(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355959
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41552112
ebirs41552112
HLIrs41552112
Exacrs41552112
Varsomers41552112
Maprs41552112
PheGenIrs41552112
hapmaprs41552112
1000 genomesrs41552112
hgdprs41552112
ensemblrs41552112
gopubmedrs41552112
geneviewrs41552112
scholarrs41552112
googlers41552112
pharmgkbrs41552112
gwascentralrs41552112
openSNPrs41552112
23andMers41552112
23andMe allrs41552112
SNP Nexus

SNPshotrs41552112
SNPdbers41552112
MSV3drs41552112
GWAS Ctlgrs41552112
GMAF0.005051
Max Magnitude0
ClinVar
Risk rs41552112(T;T)
Alt rs41552112(T;T)
Reference rs41552112(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323736T>A
CLNSRC
CLNACC