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rs151341325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341325(C;T)
Make rs151341325(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356200
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341325
dbSNP (classic)rs151341325
ClinGenrs151341325
ebirs151341325
HLIrs151341325
Exacrs151341325
Gnomadrs151341325
Varsomers151341325
LitVarrs151341325
Maprs151341325
PheGenIrs151341325
Biobankrs151341325
1000 genomesrs151341325
hgdprs151341325
ensemblrs151341325
geneviewrs151341325
scholarrs151341325
googlers151341325
pharmgkbrs151341325
gwascentralrs151341325
openSNPrs151341325
23andMers151341325
SNPshotrs151341325
SNPdbers151341325
MSV3drs151341325
GWAS Ctlgrs151341325
Max Magnitude0
ClinVar
Risk rs151341325(T;T)
Alt rs151341325(T;T)
Reference Rs151341325(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323977G>A
CLNSRC
CLNACC