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rs3819282

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3819282(A;A)
Make rs3819282(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355078
GeneHLA-B
is asnp
is mentioned by
dbSNPrs3819282
ebirs3819282
HLIrs3819282
Exacrs3819282
Varsomers3819282
Maprs3819282
PheGenIrs3819282
hapmaprs3819282
1000 genomesrs3819282
hgdprs3819282
ensemblrs3819282
gopubmedrs3819282
geneviewrs3819282
scholarrs3819282
googlers3819282
pharmgkbrs3819282
gwascentralrs3819282
openSNPrs3819282
23andMers3819282
23andMe allrs3819282
SNP Nexus

SNPshotrs3819282
SNPdbers3819282
MSV3drs3819282
GWAS Ctlgrs3819282
GMAF0.05739
Max Magnitude0
ClinVar
Risk rs3819282(A;A)
Alt rs3819282(A;A)
Reference rs3819282(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322855C>T
CLNSRC
CLNACC