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

rs151341161

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341161(C;T)
Make rs151341161(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356790
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341161
ebirs151341161
HLIrs151341161
Exacrs151341161
Varsomers151341161
Maprs151341161
PheGenIrs151341161
hapmaprs151341161
1000 genomesrs151341161
hgdprs151341161
ensemblrs151341161
gopubmedrs151341161
geneviewrs151341161
scholarrs151341161
googlers151341161
pharmgkbrs151341161
gwascentralrs151341161
openSNPrs151341161
23andMers151341161
23andMe allrs151341161
SNP Nexus

SNPshotrs151341161
SNPdbers151341161
MSV3drs151341161
GWAS Ctlgrs151341161
Max Magnitude0
ClinVar
Risk rs151341161(T;T)
Alt rs151341161(T;T)
Reference rs151341161(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324567G>A
CLNSRC
CLNACC