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rs151341169

From SNPedia

Merged intors141484466
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341169(C;T)
Make rs151341169(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356775
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341169
ebirs151341169
HLIrs151341169
Exacrs151341169
Varsomers151341169
Maprs151341169
PheGenIrs151341169
hapmaprs151341169
1000 genomesrs151341169
hgdprs151341169
ensemblrs151341169
gopubmedrs151341169
geneviewrs151341169
scholarrs151341169
googlers151341169
pharmgkbrs151341169
gwascentralrs151341169
openSNPrs151341169
23andMers151341169
23andMe allrs151341169
SNP Nexus

SNPshotrs151341169
SNPdbers151341169
MSV3drs151341169
GWAS Ctlgrs151341169
StatusMerged into rs141484466
Max Magnitude0
ClinVar
Risk rs151341169(T;T)
Alt rs151341169(T;T)
Reference rs151341169(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324552G>A
CLNSRC
CLNACC