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rs41555115

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41555115(C;T)
Make rs41555115(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356622
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555115
ebirs41555115
HLIrs41555115
Exacrs41555115
Varsomers41555115
Maprs41555115
PheGenIrs41555115
hapmaprs41555115
1000 genomesrs41555115
hgdprs41555115
ensemblrs41555115
gopubmedrs41555115
geneviewrs41555115
scholarrs41555115
googlers41555115
pharmgkbrs41555115
gwascentralrs41555115
openSNPrs41555115
23andMers41555115
23andMe allrs41555115
SNP Nexus

SNPshotrs41555115
SNPdbers41555115
MSV3drs41555115
GWAS Ctlgrs41555115
Max Magnitude0
ClinVar
Risk rs41555115(T;T)
Alt rs41555115(T;T)
Reference rs41555115(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324399G>A
CLNSRC
CLNACC