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

rs41556113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41556113(C;G)
Make rs41556113(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356452
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41556113
ebirs41556113
HLIrs41556113
Exacrs41556113
Varsomers41556113
Maprs41556113
PheGenIrs41556113
hapmaprs41556113
1000 genomesrs41556113
hgdprs41556113
ensemblrs41556113
gopubmedrs41556113
geneviewrs41556113
scholarrs41556113
googlers41556113
pharmgkbrs41556113
gwascentralrs41556113
openSNPrs41556113
23andMers41556113
23andMe allrs41556113
SNP Nexus

SNPshotrs41556113
SNPdbers41556113
MSV3drs41556113
GWAS Ctlgrs41556113
GMAF0.1212
Max Magnitude0
ClinVar
Risk rs41556113(G;G)
Alt rs41556113(G;G)
Reference rs41556113(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324229G>C
CLNSRC
CLNACC