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

rs151341231

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341231(A;A)
Make rs151341231(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356386
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341231
ebirs151341231
HLIrs151341231
Exacrs151341231
Varsomers151341231
Maprs151341231
PheGenIrs151341231
hapmaprs151341231
1000 genomesrs151341231
hgdprs151341231
ensemblrs151341231
gopubmedrs151341231
geneviewrs151341231
scholarrs151341231
googlers151341231
pharmgkbrs151341231
gwascentralrs151341231
openSNPrs151341231
23andMers151341231
23andMe allrs151341231
SNP Nexus

SNPshotrs151341231
SNPdbers151341231
MSV3drs151341231
GWAS Ctlgrs151341231
Max Magnitude0
ClinVar
Risk rs151341231(A;A)
Alt rs151341231(A;A)
Reference rs151341231(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324163G>T
CLNSRC
CLNACC