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rs41555918

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41555918(C;C)
Make rs41555918(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356940
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555918
ebirs41555918
HLIrs41555918
Exacrs41555918
Varsomers41555918
Maprs41555918
PheGenIrs41555918
hapmaprs41555918
1000 genomesrs41555918
hgdprs41555918
ensemblrs41555918
gopubmedrs41555918
geneviewrs41555918
scholarrs41555918
googlers41555918
pharmgkbrs41555918
gwascentralrs41555918
openSNPrs41555918
23andMers41555918
23andMe allrs41555918
SNP Nexus

SNPshotrs41555918
SNPdbers41555918
MSV3drs41555918
GWAS Ctlgrs41555918
Max Magnitude0
ClinVar
Risk rs41555918(C;C)
Alt rs41555918(C;C)
Reference rs41555918(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324717A>G
CLNSRC
CLNACC