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rs151341186

From SNPedia

Merged intors151341185
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341186(C;T)
Make rs151341186(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356766
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341186
ebirs151341186
HLIrs151341186
Exacrs151341186
Varsomers151341186
Maprs151341186
PheGenIrs151341186
hapmaprs151341186
1000 genomesrs151341186
hgdprs151341186
ensemblrs151341186
gopubmedrs151341186
geneviewrs151341186
scholarrs151341186
googlers151341186
pharmgkbrs151341186
gwascentralrs151341186
openSNPrs151341186
23andMers151341186
23andMe allrs151341186
SNP Nexus

SNPshotrs151341186
SNPdbers151341186
MSV3drs151341186
GWAS Ctlgrs151341186
StatusMerged into rs151341185
Max Magnitude0
ClinVar
Risk rs151341186(T;T)
Alt rs151341186(T;T)
Reference rs151341186(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324543G>A
CLNSRC
CLNACC