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rs151341390

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341390(A;T)
Make rs151341390(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355165
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341390
dbSNP (classic)rs151341390
ClinGenrs151341390
ebirs151341390
HLIrs151341390
Exacrs151341390
Gnomadrs151341390
Varsomers151341390
LitVarrs151341390
Maprs151341390
PheGenIrs151341390
Biobankrs151341390
1000 genomesrs151341390
hgdprs151341390
ensemblrs151341390
geneviewrs151341390
scholarrs151341390
googlers151341390
pharmgkbrs151341390
gwascentralrs151341390
openSNPrs151341390
23andMers151341390
SNPshotrs151341390
SNPdbers151341390
MSV3drs151341390
GWAS Ctlgrs151341390
Max Magnitude0
ClinVar
Risk rs151341390(T;T)
Alt rs151341390(T;T)
Reference Rs151341390(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322942T>A
CLNSRC
CLNACC