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rs41543613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs41543613(C;T)
Make rs41543613(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355433
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41543613
ebirs41543613
HLIrs41543613
Exacrs41543613
Varsomers41543613
Maprs41543613
PheGenIrs41543613
hapmaprs41543613
1000 genomesrs41543613
hgdprs41543613
ensemblrs41543613
gopubmedrs41543613
geneviewrs41543613
scholarrs41543613
googlers41543613
pharmgkbrs41543613
gwascentralrs41543613
openSNPrs41543613
23andMers41543613
23andMe allrs41543613
SNP Nexus

SNPshotrs41543613
SNPdbers41543613
MSV3drs41543613
GWAS Ctlgrs41543613
Max Magnitude0
ClinVar
Risk rs41543613(T;T)
Alt rs41543613(T;T)
Reference rs41543613(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323210G>A
CLNSRC
CLNACC