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rs41555623

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41555623(A;A)
Make rs41555623(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355156
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41555623
ebirs41555623
HLIrs41555623
Exacrs41555623
Varsomers41555623
Maprs41555623
PheGenIrs41555623
hapmaprs41555623
1000 genomesrs41555623
hgdprs41555623
ensemblrs41555623
gopubmedrs41555623
geneviewrs41555623
scholarrs41555623
googlers41555623
pharmgkbrs41555623
gwascentralrs41555623
openSNPrs41555623
23andMers41555623
23andMe allrs41555623
SNP Nexus

SNPshotrs41555623
SNPdbers41555623
MSV3drs41555623
GWAS Ctlgrs41555623
Max Magnitude0
ClinVar
Risk rs41555623(A;A)
Alt rs41555623(A;A)
Reference rs41555623(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322933C>T
CLNSRC
CLNACC