Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341346

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341346(C;C)
Make rs151341346(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355527
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341346
dbSNP (classic)rs151341346
ClinGenrs151341346
ebirs151341346
HLIrs151341346
Exacrs151341346
Gnomadrs151341346
Varsomers151341346
LitVarrs151341346
Maprs151341346
PheGenIrs151341346
Biobankrs151341346
1000 genomesrs151341346
hgdprs151341346
ensemblrs151341346
geneviewrs151341346
scholarrs151341346
googlers151341346
pharmgkbrs151341346
gwascentralrs151341346
openSNPrs151341346
23andMers151341346
SNPshotrs151341346
SNPdbers151341346
MSV3drs151341346
GWAS Ctlgrs151341346
Max Magnitude0
ClinVar
Risk rs151341346(C;C)
Alt rs151341346(C;C)
Reference Rs151341346(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323304C>G
CLNSRC
CLNACC