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rs3819306

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs3819306(C;C)
Make rs3819306(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354356
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819306
dbSNP (classic)rs3819306
ClinGenrs3819306
ebirs3819306
HLIrs3819306
Exacrs3819306
Gnomadrs3819306
Varsomers3819306
LitVarrs3819306
Maprs3819306
PheGenIrs3819306
Biobankrs3819306
1000 genomesrs3819306
hgdprs3819306
ensemblrs3819306
geneviewrs3819306
scholarrs3819306
googlers3819306
pharmgkbrs3819306
gwascentralrs3819306
openSNPrs3819306
23andMers3819306
SNPshotrs3819306
SNPdbers3819306
MSV3drs3819306
GWAS Ctlgrs3819306
GMAF0.461
Max Magnitude0
ClinVar
Risk rs3819306(C;C)
Alt rs3819306(C;C)
Reference Rs3819306(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322133A>G
CLNSRC
CLNACC