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rs41550818

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41550818(A;C)
Make rs41550818(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355904
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41550818
ebirs41550818
HLIrs41550818
Exacrs41550818
Varsomers41550818
Maprs41550818
PheGenIrs41550818
hapmaprs41550818
1000 genomesrs41550818
hgdprs41550818
ensemblrs41550818
gopubmedrs41550818
geneviewrs41550818
scholarrs41550818
googlers41550818
pharmgkbrs41550818
gwascentralrs41550818
openSNPrs41550818
23andMers41550818
23andMe allrs41550818
SNP Nexus

SNPshotrs41550818
SNPdbers41550818
MSV3drs41550818
GWAS Ctlgrs41550818
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41550818(C;C)
Alt rs41550818(C;C)
Reference rs41550818(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323681T>G
CLNSRC
CLNACC