Have questions? Visit https://www.reddit.com/r/SNPedia

rs41559118

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41559118(A;A)
Make rs41559118(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356449
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41559118
ebirs41559118
HLIrs41559118
Exacrs41559118
Varsomers41559118
Maprs41559118
PheGenIrs41559118
hapmaprs41559118
1000 genomesrs41559118
hgdprs41559118
ensemblrs41559118
gopubmedrs41559118
geneviewrs41559118
scholarrs41559118
googlers41559118
pharmgkbrs41559118
gwascentralrs41559118
openSNPrs41559118
23andMers41559118
23andMe allrs41559118
SNP Nexus

SNPshotrs41559118
SNPdbers41559118
MSV3drs41559118
GWAS Ctlgrs41559118
Max Magnitude0
ClinVar
Risk rs41559118(A;A)
Alt rs41559118(A;A)
Reference rs41559118(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324226C>T
CLNSRC
CLNACC