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rs41547715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41547715(G;T)
Make rs41547715(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355935
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41547715
ebirs41547715
HLIrs41547715
Exacrs41547715
Varsomers41547715
Maprs41547715
PheGenIrs41547715
hapmaprs41547715
1000 genomesrs41547715
hgdprs41547715
ensemblrs41547715
gopubmedrs41547715
geneviewrs41547715
scholarrs41547715
googlers41547715
pharmgkbrs41547715
gwascentralrs41547715
openSNPrs41547715
23andMers41547715
23andMe allrs41547715
SNP Nexus

SNPshotrs41547715
SNPdbers41547715
MSV3drs41547715
GWAS Ctlgrs41547715
GMAF0.0009183
Max Magnitude0
ClinVar
Risk rs41547715(T;T)
Alt rs41547715(T;T)
Reference rs41547715(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323712C>A
CLNSRC
CLNACC