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rs41545312

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs41545312(A;G)
Make rs41545312(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356361
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545312
ebirs41545312
HLIrs41545312
Exacrs41545312
Varsomers41545312
Maprs41545312
PheGenIrs41545312
hapmaprs41545312
1000 genomesrs41545312
hgdprs41545312
ensemblrs41545312
gopubmedrs41545312
geneviewrs41545312
scholarrs41545312
googlers41545312
pharmgkbrs41545312
gwascentralrs41545312
openSNPrs41545312
23andMers41545312
23andMe allrs41545312
SNP Nexus

SNPshotrs41545312
SNPdbers41545312
MSV3drs41545312
GWAS Ctlgrs41545312
Max Magnitude0
ClinVar
Risk rs41545312(G;G)
Alt rs41545312(G;G)
Reference rs41545312(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324138T>C
CLNSRC
CLNACC