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

rs151341251

From SNPedia

Merged intors1050370
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341251(A;A)
Make rs151341251(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356312
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341251
ebirs151341251
HLIrs151341251
Exacrs151341251
Varsomers151341251
Maprs151341251
PheGenIrs151341251
hapmaprs151341251
1000 genomesrs151341251
hgdprs151341251
ensemblrs151341251
gopubmedrs151341251
geneviewrs151341251
scholarrs151341251
googlers151341251
pharmgkbrs151341251
gwascentralrs151341251
openSNPrs151341251
23andMers151341251
23andMe allrs151341251
SNP Nexus

SNPshotrs151341251
SNPdbers151341251
MSV3drs151341251
GWAS Ctlgrs151341251
StatusMerged into rs1050370
Max Magnitude0
ClinVar
Risk rs151341251(A;A)
Alt rs151341251(A;A)
Reference rs151341251(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324089G>T
CLNSRC
CLNACC