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

rs151341358

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341358(G;T)
Make rs151341358(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355386
GeneHLA-B, MIR6891
is asnp
is mentioned by
dbSNPrs151341358
dbSNP (classic)rs151341358
ClinGenrs151341358
ebirs151341358
HLIrs151341358
Exacrs151341358
Gnomadrs151341358
Varsomers151341358
LitVarrs151341358
Maprs151341358
PheGenIrs151341358
Biobankrs151341358
1000 genomesrs151341358
hgdprs151341358
ensemblrs151341358
geneviewrs151341358
scholarrs151341358
googlers151341358
pharmgkbrs151341358
gwascentralrs151341358
openSNPrs151341358
23andMers151341358
SNPshotrs151341358
SNPdbers151341358
MSV3drs151341358
GWAS Ctlgrs151341358
Max Magnitude0
ClinVar
Risk rs151341358(T;T)
Alt rs151341358(T;T)
Reference Rs151341358(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323163C>A
CLNSRC
CLNACC