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rs41545813

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41545813(C;T)
Make rs41545813(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356357
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41545813
ebirs41545813
HLIrs41545813
Exacrs41545813
Varsomers41545813
Maprs41545813
PheGenIrs41545813
hapmaprs41545813
1000 genomesrs41545813
hgdprs41545813
ensemblrs41545813
gopubmedrs41545813
geneviewrs41545813
scholarrs41545813
googlers41545813
pharmgkbrs41545813
gwascentralrs41545813
openSNPrs41545813
23andMers41545813
23andMe allrs41545813
SNP Nexus

SNPshotrs41545813
SNPdbers41545813
MSV3drs41545813
GWAS Ctlgrs41545813
Max Magnitude0
ClinVar
Risk rs41545813(T;T)
Alt rs41545813(T;T)
Reference rs41545813(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324134G>A
CLNSRC
CLNACC