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rs3819285

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3819285(A;A)
Make rs3819285(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354965
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs3819285
dbSNP (classic)rs3819285
ClinGenrs3819285
ebirs3819285
HLIrs3819285
Exacrs3819285
Gnomadrs3819285
Varsomers3819285
LitVarrs3819285
Maprs3819285
PheGenIrs3819285
Biobankrs3819285
1000 genomesrs3819285
hgdprs3819285
ensemblrs3819285
geneviewrs3819285
scholarrs3819285
googlers3819285
pharmgkbrs3819285
gwascentralrs3819285
openSNPrs3819285
23andMers3819285
SNPshotrs3819285
SNPdbers3819285
MSV3drs3819285
GWAS Ctlgrs3819285
GMAF0.03444
Max Magnitude0
ClinVar
Risk rs3819285(A;A)
Alt rs3819285(A;A)
Reference Rs3819285(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322742G>T
CLNSRC
CLNACC