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rs41545619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41545619(A;A)
Make rs41545619(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356599
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545619
ebirs41545619
HLIrs41545619
Exacrs41545619
Varsomers41545619
Maprs41545619
PheGenIrs41545619
hapmaprs41545619
1000 genomesrs41545619
hgdprs41545619
ensemblrs41545619
gopubmedrs41545619
geneviewrs41545619
scholarrs41545619
googlers41545619
pharmgkbrs41545619
gwascentralrs41545619
openSNPrs41545619
23andMers41545619
23andMe allrs41545619
SNP Nexus

SNPshotrs41545619
SNPdbers41545619
MSV3drs41545619
GWAS Ctlgrs41545619
Max Magnitude0
ClinVar
Risk rs41545619(A;A)
Alt rs41545619(A;A)
Reference rs41545619(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324376C>T
CLNSRC
CLNACC