Have questions? Visit https://www.reddit.com/r/SNPedia

rs3819284

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3819284(C;T)
Make rs3819284(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354990
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819284
ebirs3819284
HLIrs3819284
Exacrs3819284
Varsomers3819284
Maprs3819284
PheGenIrs3819284
hapmaprs3819284
1000 genomesrs3819284
hgdprs3819284
ensemblrs3819284
gopubmedrs3819284
geneviewrs3819284
scholarrs3819284
googlers3819284
pharmgkbrs3819284
gwascentralrs3819284
openSNPrs3819284
23andMers3819284
23andMe allrs3819284
SNP Nexus

SNPshotrs3819284
SNPdbers3819284
MSV3drs3819284
GWAS Ctlgrs3819284
GMAF0.03306
Max Magnitude0
? (C;C) (C;T) (T;T) 28
ClinVar
Risk rs3819284(T;T)
Alt rs3819284(T;T)
Reference rs3819284(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322767G>A
CLNSRC
CLNACC