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rs151341194

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341194(C;T)
Make rs151341194(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356745
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341194
ebirs151341194
HLIrs151341194
Exacrs151341194
Varsomers151341194
Maprs151341194
PheGenIrs151341194
hapmaprs151341194
1000 genomesrs151341194
hgdprs151341194
ensemblrs151341194
gopubmedrs151341194
geneviewrs151341194
scholarrs151341194
googlers151341194
pharmgkbrs151341194
gwascentralrs151341194
openSNPrs151341194
23andMers151341194
23andMe allrs151341194
SNP Nexus

SNPshotrs151341194
SNPdbers151341194
MSV3drs151341194
GWAS Ctlgrs151341194
Max Magnitude0
ClinVar
Risk rs151341194(T;T)
Alt rs151341194(T;T)
Reference rs151341194(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324522G>A
CLNSRC
CLNACC