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rs151341321

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341321(C;T)
Make rs151341321(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356212
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341321
dbSNP (classic)rs151341321
ClinGenrs151341321
ebirs151341321
HLIrs151341321
Exacrs151341321
Gnomadrs151341321
Varsomers151341321
LitVarrs151341321
Maprs151341321
PheGenIrs151341321
Biobankrs151341321
1000 genomesrs151341321
hgdprs151341321
ensemblrs151341321
geneviewrs151341321
scholarrs151341321
googlers151341321
pharmgkbrs151341321
gwascentralrs151341321
openSNPrs151341321
23andMers151341321
SNPshotrs151341321
SNPdbers151341321
MSV3drs151341321
GWAS Ctlgrs151341321
Max Magnitude0
ClinVar
Risk rs151341321(T;T)
Alt rs151341321(T;T)
Reference Rs151341321(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323989G>A
CLNSRC
CLNACC