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

rs41558116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558116(A;A)
Make rs41558116(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355398
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558116
ebirs41558116
HLIrs41558116
Exacrs41558116
Varsomers41558116
Maprs41558116
PheGenIrs41558116
hapmaprs41558116
1000 genomesrs41558116
hgdprs41558116
ensemblrs41558116
gopubmedrs41558116
geneviewrs41558116
scholarrs41558116
googlers41558116
pharmgkbrs41558116
gwascentralrs41558116
openSNPrs41558116
23andMers41558116
23andMe allrs41558116
SNP Nexus

SNPshotrs41558116
SNPdbers41558116
MSV3drs41558116
GWAS Ctlgrs41558116
Max Magnitude0
ClinVar
Risk rs41558116(A;A)
Alt rs41558116(A;A)
Reference rs41558116(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323175C>T
CLNSRC
CLNACC