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

rs151341166

From SNPedia

Merged intors151341165
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341166(C;G)
Make rs151341166(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356776
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341166
ebirs151341166
HLIrs151341166
Exacrs151341166
Varsomers151341166
Maprs151341166
PheGenIrs151341166
hapmaprs151341166
1000 genomesrs151341166
hgdprs151341166
ensemblrs151341166
gopubmedrs151341166
geneviewrs151341166
scholarrs151341166
googlers151341166
pharmgkbrs151341166
gwascentralrs151341166
openSNPrs151341166
23andMers151341166
23andMe allrs151341166
SNP Nexus

SNPshotrs151341166
SNPdbers151341166
MSV3drs151341166
GWAS Ctlgrs151341166
StatusMerged into rs151341165
Max Magnitude0
ClinVar
Risk rs151341166(G;G)
Alt rs151341166(G;G)
Reference rs151341166(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324553G>C
CLNSRC
CLNACC