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rs151341090

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341090(G;G)
Make rs151341090(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356949
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341090
dbSNP (classic)rs151341090
ClinGenrs151341090
ebirs151341090
HLIrs151341090
Exacrs151341090
Gnomadrs151341090
Varsomers151341090
LitVarrs151341090
Maprs151341090
PheGenIrs151341090
Biobankrs151341090
1000 genomesrs151341090
hgdprs151341090
ensemblrs151341090
geneviewrs151341090
scholarrs151341090
googlers151341090
pharmgkbrs151341090
gwascentralrs151341090
openSNPrs151341090
23andMers151341090
SNPshotrs151341090
SNPdbers151341090
MSV3drs151341090
GWAS Ctlgrs151341090
Max Magnitude0
ClinVar
Risk rs151341090(G;G)
Alt rs151341090(G;G)
Reference Rs151341090(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324726A>C
CLNSRC
CLNACC