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rs3819292

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3819292(G;T)
Make rs3819292(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354745
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819292
ebirs3819292
HLIrs3819292
Exacrs3819292
Varsomers3819292
Maprs3819292
PheGenIrs3819292
hapmaprs3819292
1000 genomesrs3819292
hgdprs3819292
ensemblrs3819292
gopubmedrs3819292
geneviewrs3819292
scholarrs3819292
googlers3819292
pharmgkbrs3819292
gwascentralrs3819292
openSNPrs3819292
23andMers3819292
23andMe allrs3819292
SNP Nexus

SNPshotrs3819292
SNPdbers3819292
MSV3drs3819292
GWAS Ctlgrs3819292
GMAF0.1974
Max Magnitude0
ClinVar
Risk rs3819292(T;T)
Alt rs3819292(T;T)
Reference rs3819292(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322522C>A
CLNSRC
CLNACC