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rs41553914

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553914(C;T)
Make rs41553914(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355809
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553914
ebirs41553914
HLIrs41553914
Exacrs41553914
Varsomers41553914
Maprs41553914
PheGenIrs41553914
hapmaprs41553914
1000 genomesrs41553914
hgdprs41553914
ensemblrs41553914
gopubmedrs41553914
geneviewrs41553914
scholarrs41553914
googlers41553914
pharmgkbrs41553914
gwascentralrs41553914
openSNPrs41553914
23andMers41553914
23andMe allrs41553914
SNP Nexus

SNPshotrs41553914
SNPdbers41553914
MSV3drs41553914
GWAS Ctlgrs41553914
GMAF0.002296
Max Magnitude0
ClinVar
Risk rs41553914(T;T)
Alt rs41553914(T;T)
Reference rs41553914(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323586G>A
CLNSRC
CLNACC