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rs41553413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41553413(A;A)
Make rs41553413(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355508
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41553413
ebirs41553413
HLIrs41553413
Exacrs41553413
Varsomers41553413
Maprs41553413
PheGenIrs41553413
hapmaprs41553413
1000 genomesrs41553413
hgdprs41553413
ensemblrs41553413
gopubmedrs41553413
geneviewrs41553413
scholarrs41553413
googlers41553413
pharmgkbrs41553413
gwascentralrs41553413
openSNPrs41553413
23andMers41553413
23andMe allrs41553413
SNP Nexus

SNPshotrs41553413
SNPdbers41553413
MSV3drs41553413
GWAS Ctlgrs41553413
Max Magnitude0
ClinVar
Risk rs41553413(A,G,T;A,G,T)
Alt rs41553413(A,G,T;A,G,T)
Reference rs41553413(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323285G>A; NC_000006.11:g.31323285G>C; NC_000006.11:g.31323285G>T
CLNSRC
CLNACC