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

rs41540113

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs41540113(C;C)
Make rs41540113(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356709
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41540113
ebirs41540113
HLIrs41540113
Exacrs41540113
Varsomers41540113
Maprs41540113
PheGenIrs41540113
hapmaprs41540113
1000 genomesrs41540113
hgdprs41540113
ensemblrs41540113
gopubmedrs41540113
geneviewrs41540113
scholarrs41540113
googlers41540113
pharmgkbrs41540113
gwascentralrs41540113
openSNPrs41540113
23andMers41540113
23andMe allrs41540113
SNP Nexus

SNPshotrs41540113
SNPdbers41540113
MSV3drs41540113
GWAS Ctlgrs41540113
Max Magnitude0
ClinVar
Risk rs41540113(C,G;C,G)
Alt rs41540113(C,G;C,G)
Reference rs41540113(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324486A>C; NC_000006.11:g.31324486A>G
CLNSRC
CLNACC