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rs151341352

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341352(C;T)
Make rs151341352(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355452
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341352
dbSNP (classic)rs151341352
ClinGenrs151341352
ebirs151341352
HLIrs151341352
Exacrs151341352
Gnomadrs151341352
Varsomers151341352
LitVarrs151341352
Maprs151341352
PheGenIrs151341352
Biobankrs151341352
1000 genomesrs151341352
hgdprs151341352
ensemblrs151341352
geneviewrs151341352
scholarrs151341352
googlers151341352
pharmgkbrs151341352
gwascentralrs151341352
openSNPrs151341352
23andMers151341352
SNPshotrs151341352
SNPdbers151341352
MSV3drs151341352
GWAS Ctlgrs151341352
Max Magnitude0
ClinVar
Risk rs151341352(T;T)
Alt rs151341352(T;T)
Reference Rs151341352(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323229G>A
CLNSRC
CLNACC