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rs41550413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41550413(-;-)
Make rs41550413(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355724
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41550413
ebirs41550413
HLIrs41550413
Exacrs41550413
Varsomers41550413
Maprs41550413
PheGenIrs41550413
hapmaprs41550413
1000 genomesrs41550413
hgdprs41550413
ensemblrs41550413
gopubmedrs41550413
geneviewrs41550413
scholarrs41550413
googlers41550413
pharmgkbrs41550413
gwascentralrs41550413
openSNPrs41550413
23andMers41550413
23andMe allrs41550413
SNP Nexus

SNPshotrs41550413
SNPdbers41550413
MSV3drs41550413
GWAS Ctlgrs41550413
Max Magnitude0
ClinVar
Risk rs41550413(;)
Alt rs41550413(;)
Reference rs41550413(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323501delC
CLNSRC
CLNACC