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rs41555419

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555419(C;T)
Make rs41555419(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355332
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555419
ebirs41555419
HLIrs41555419
Exacrs41555419
Varsomers41555419
Maprs41555419
PheGenIrs41555419
hapmaprs41555419
1000 genomesrs41555419
hgdprs41555419
ensemblrs41555419
gopubmedrs41555419
geneviewrs41555419
scholarrs41555419
googlers41555419
pharmgkbrs41555419
gwascentralrs41555419
openSNPrs41555419
23andMers41555419
23andMe allrs41555419
SNP Nexus

SNPshotrs41555419
SNPdbers41555419
MSV3drs41555419
GWAS Ctlgrs41555419
Max Magnitude0
ClinVar
Risk rs41555419(T;T)
Alt rs41555419(T;T)
Reference rs41555419(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323109G>A
CLNSRC
CLNACC