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rs41555216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555216(C;T)
Make rs41555216(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356948
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555216
ebirs41555216
HLIrs41555216
Exacrs41555216
Varsomers41555216
Maprs41555216
PheGenIrs41555216
hapmaprs41555216
1000 genomesrs41555216
hgdprs41555216
ensemblrs41555216
gopubmedrs41555216
geneviewrs41555216
scholarrs41555216
googlers41555216
pharmgkbrs41555216
gwascentralrs41555216
openSNPrs41555216
23andMers41555216
23andMe allrs41555216
SNP Nexus

SNPshotrs41555216
SNPdbers41555216
MSV3drs41555216
GWAS Ctlgrs41555216
GMAF0.003214
Max Magnitude0
ClinVar
Risk rs41555216(T;T)
Alt rs41555216(T;T)
Reference rs41555216(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324725G>A
CLNSRC
CLNACC