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rs3819276

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3819276(A;A)
Make rs3819276(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355250
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819276
ebirs3819276
HLIrs3819276
Exacrs3819276
Varsomers3819276
Maprs3819276
PheGenIrs3819276
hapmaprs3819276
1000 genomesrs3819276
hgdprs3819276
ensemblrs3819276
gopubmedrs3819276
geneviewrs3819276
scholarrs3819276
googlers3819276
pharmgkbrs3819276
gwascentralrs3819276
openSNPrs3819276
23andMers3819276
23andMe allrs3819276
SNP Nexus

SNPshotrs3819276
SNPdbers3819276
MSV3drs3819276
GWAS Ctlgrs3819276
GMAF0.006887
Max Magnitude0
ClinVar
Risk rs3819276(A;A)
Alt rs3819276(A;A)
Reference rs3819276(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323027C>T
CLNSRC
CLNACC