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rs11546719

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11546719(A;A)
Make rs11546719(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356897
GeneHLA-B
is asnp
is mentioned by
dbSNPrs11546719
ebirs11546719
HLIrs11546719
Exacrs11546719
Varsomers11546719
Maprs11546719
PheGenIrs11546719
hapmaprs11546719
1000 genomesrs11546719
hgdprs11546719
ensemblrs11546719
gopubmedrs11546719
geneviewrs11546719
scholarrs11546719
googlers11546719
pharmgkbrs11546719
gwascentralrs11546719
openSNPrs11546719
23andMers11546719
23andMe allrs11546719
SNP Nexus

SNPshotrs11546719
SNPdbers11546719
MSV3drs11546719
GWAS Ctlgrs11546719
GMAF0.02617
Max Magnitude0
ClinVar
Risk rs11546719(A,C,T;A,C,T)
Alt rs11546719(A,C,T;A,C,T)
Reference rs11546719(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324674C>A; NC_000006.11:g.31324674C>G; NC_000006.11:g.31324674C>T
CLNSRC
CLNACC