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

rs151341391

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs151341391(-;-)
Make rs151341391(-;GTG)
Make rs151341391(GTG;GTG)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31322941
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341391
ebirs151341391
HLIrs151341391
Exacrs151341391
Varsomers151341391
Maprs151341391
PheGenIrs151341391
hapmaprs151341391
1000 genomesrs151341391
hgdprs151341391
ensemblrs151341391
gopubmedrs151341391
geneviewrs151341391
scholarrs151341391
googlers151341391
pharmgkbrs151341391
gwascentralrs151341391
openSNPrs151341391
23andMers151341391
23andMe allrs151341391
SNP Nexus

SNPshotrs151341391
SNPdbers151341391
MSV3drs151341391
GWAS Ctlgrs151341391
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341391(TGG;TGG)
Alt rs151341391(TGG;TGG)
Reference rs151341391(;)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322941_31322942insCAC
CLNSRC
CLNACC