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rs3819288

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3819288(A;G)
Make rs3819288(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354917
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs3819288
dbSNP (classic)rs3819288
ClinGenrs3819288
ebirs3819288
HLIrs3819288
Exacrs3819288
Gnomadrs3819288
Varsomers3819288
LitVarrs3819288
Maprs3819288
PheGenIrs3819288
Biobankrs3819288
1000 genomesrs3819288
hgdprs3819288
ensemblrs3819288
geneviewrs3819288
scholarrs3819288
googlers3819288
pharmgkbrs3819288
gwascentralrs3819288
openSNPrs3819288
23andMers3819288
SNPshotrs3819288
SNPdbers3819288
MSV3drs3819288
GWAS Ctlgrs3819288
Max Magnitude0
ClinVar
Risk rs3819288(G;G)
Alt rs3819288(G;G)
Reference Rs3819288(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322694T>C
CLNSRC
CLNACC