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

rs41558112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41558112(A;A)
Make rs41558112(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356356
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41558112
ebirs41558112
HLIrs41558112
Exacrs41558112
Varsomers41558112
Maprs41558112
PheGenIrs41558112
hapmaprs41558112
1000 genomesrs41558112
hgdprs41558112
ensemblrs41558112
gopubmedrs41558112
geneviewrs41558112
scholarrs41558112
googlers41558112
pharmgkbrs41558112
gwascentralrs41558112
openSNPrs41558112
23andMers41558112
23andMe allrs41558112
SNP Nexus

SNPshotrs41558112
SNPdbers41558112
MSV3drs41558112
GWAS Ctlgrs41558112
Max Magnitude0
ClinVar
Risk rs41558112(A,C;A,C)
Alt rs41558112(A,C;A,C)
Reference rs41558112(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324133C>G; NC_000006.11:g.31324133C>T
CLNSRC
CLNACC