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rs41543219

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41543219(A;A)
Make rs41543219(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356612
GeneHLA-B
is asnp
is mentioned by
dbSNPrs41543219
ebirs41543219
HLIrs41543219
Exacrs41543219
Varsomers41543219
Maprs41543219
PheGenIrs41543219
hapmaprs41543219
1000 genomesrs41543219
hgdprs41543219
ensemblrs41543219
gopubmedrs41543219
geneviewrs41543219
scholarrs41543219
googlers41543219
pharmgkbrs41543219
gwascentralrs41543219
openSNPrs41543219
23andMers41543219
23andMe allrs41543219
SNP Nexus

SNPshotrs41543219
SNPdbers41543219
MSV3drs41543219
GWAS Ctlgrs41543219
Max Magnitude0
ClinVar
Risk rs41543219(A;A)
Alt rs41543219(A;A)
Reference rs41543219(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324389C>T
CLNSRC
CLNACC