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rs12528645

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs12528645(C;C)
Make rs12528645(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355948
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs12528645
dbSNP (classic)rs12528645
ClinGenrs12528645
ebirs12528645
HLIrs12528645
Exacrs12528645
Gnomadrs12528645
Varsomers12528645
LitVarrs12528645
Maprs12528645
PheGenIrs12528645
Biobankrs12528645
1000 genomesrs12528645
hgdprs12528645
ensemblrs12528645
geneviewrs12528645
scholarrs12528645
googlers12528645
pharmgkbrs12528645
gwascentralrs12528645
openSNPrs12528645
23andMers12528645
SNPshotrs12528645
SNPdbers12528645
MSV3drs12528645
GWAS Ctlgrs12528645
GMAF0.1221
Max Magnitude0
ClinVar
Risk rs12528645(C;C)
Alt rs12528645(C;C)
Reference Rs12528645(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31323725T>C
CLNSRC
CLNACC