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rs41550022

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41550022(-;-)
Make rs41550022(-;T)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324585
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41550022
ebirs41550022
HLIrs41550022
Exacrs41550022
Varsomers41550022
Maprs41550022
PheGenIrs41550022
hapmaprs41550022
1000 genomesrs41550022
hgdprs41550022
ensemblrs41550022
gopubmedrs41550022
geneviewrs41550022
scholarrs41550022
googlers41550022
pharmgkbrs41550022
gwascentralrs41550022
openSNPrs41550022
23andMers41550022
23andMe allrs41550022
SNP Nexus

SNPshotrs41550022
SNPdbers41550022
MSV3drs41550022
GWAS Ctlgrs41550022
StatusDeleted
Max Magnitude0
ClinVar
Risk rs41550022(;)
Alt rs41550022(;)
Reference rs41550022(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324585delA
CLNSRC
CLNACC