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rs41550513

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41550513(G;G)
Make rs41550513(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354539
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41550513
ebirs41550513
HLIrs41550513
Exacrs41550513
Varsomers41550513
Maprs41550513
PheGenIrs41550513
hapmaprs41550513
1000 genomesrs41550513
hgdprs41550513
ensemblrs41550513
gopubmedrs41550513
geneviewrs41550513
scholarrs41550513
googlers41550513
pharmgkbrs41550513
gwascentralrs41550513
openSNPrs41550513
23andMers41550513
23andMe allrs41550513
SNP Nexus

SNPshotrs41550513
SNPdbers41550513
MSV3drs41550513
GWAS Ctlgrs41550513
Max Magnitude0
ClinVar
Risk rs41550513(G;G)
Alt rs41550513(G;G)
Reference rs41550513(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322316A>C
CLNSRC
CLNACC