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rs3819294

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3819294(C;T)
Make rs3819294(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354710
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819294
ebirs3819294
HLIrs3819294
Exacrs3819294
Varsomers3819294
Maprs3819294
PheGenIrs3819294
hapmaprs3819294
1000 genomesrs3819294
hgdprs3819294
ensemblrs3819294
gopubmedrs3819294
geneviewrs3819294
scholarrs3819294
googlers3819294
pharmgkbrs3819294
gwascentralrs3819294
openSNPrs3819294
23andMers3819294
23andMe allrs3819294
SNP Nexus

SNPshotrs3819294
SNPdbers3819294
MSV3drs3819294
GWAS Ctlgrs3819294
GMAF0.1276
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs3819294(T;T)
Alt rs3819294(T;T)
Reference rs3819294(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322487G>A
CLNSRC
CLNACC