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rs41559119

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41559119(A;G)
Make rs41559119(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355225
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559119
ebirs41559119
HLIrs41559119
Exacrs41559119
Varsomers41559119
Maprs41559119
PheGenIrs41559119
hapmaprs41559119
1000 genomesrs41559119
hgdprs41559119
ensemblrs41559119
gopubmedrs41559119
geneviewrs41559119
scholarrs41559119
googlers41559119
pharmgkbrs41559119
gwascentralrs41559119
openSNPrs41559119
23andMers41559119
23andMe allrs41559119
SNP Nexus

SNPshotrs41559119
SNPdbers41559119
MSV3drs41559119
GWAS Ctlgrs41559119
Max Magnitude0
ClinVar
Risk rs41559119(G;G)
Alt rs41559119(G;G)
Reference rs41559119(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323002T>C
CLNSRC
CLNACC