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rs151341249

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341249(A;T)
Make rs151341249(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356314
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341249
dbSNP (classic)rs151341249
ClinGenrs151341249
ebirs151341249
HLIrs151341249
Exacrs151341249
Gnomadrs151341249
Varsomers151341249
LitVarrs151341249
Maprs151341249
PheGenIrs151341249
Biobankrs151341249
1000 genomesrs151341249
hgdprs151341249
ensemblrs151341249
geneviewrs151341249
scholarrs151341249
googlers151341249
pharmgkbrs151341249
gwascentralrs151341249
openSNPrs151341249
23andMers151341249
SNPshotrs151341249
SNPdbers151341249
MSV3drs151341249
GWAS Ctlgrs151341249
Max Magnitude0
ClinVar
Risk rs151341249(T;T)
Alt rs151341249(T;T)
Reference Rs151341249(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324091T>A
CLNSRC
CLNACC