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rs41546016

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41546016(A;G)
Make rs41546016(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355366
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41546016
ebirs41546016
HLIrs41546016
Exacrs41546016
Varsomers41546016
Maprs41546016
PheGenIrs41546016
hapmaprs41546016
1000 genomesrs41546016
hgdprs41546016
ensemblrs41546016
gopubmedrs41546016
geneviewrs41546016
scholarrs41546016
googlers41546016
pharmgkbrs41546016
gwascentralrs41546016
openSNPrs41546016
23andMers41546016
23andMe allrs41546016
SNP Nexus

SNPshotrs41546016
SNPdbers41546016
MSV3drs41546016
GWAS Ctlgrs41546016
Max Magnitude0
ClinVar
Risk rs41546016(G;G)
Alt rs41546016(G;G)
Reference rs41546016(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323143T>C
CLNSRC
CLNACC