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rs151341193

From SNPedia

Merged intors151341192
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341193(A;G)
Make rs151341193(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356763
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341193
ebirs151341193
HLIrs151341193
Exacrs151341193
Varsomers151341193
Maprs151341193
PheGenIrs151341193
hapmaprs151341193
1000 genomesrs151341193
hgdprs151341193
ensemblrs151341193
gopubmedrs151341193
geneviewrs151341193
scholarrs151341193
googlers151341193
pharmgkbrs151341193
gwascentralrs151341193
openSNPrs151341193
23andMers151341193
23andMe allrs151341193
SNP Nexus

SNPshotrs151341193
SNPdbers151341193
MSV3drs151341193
GWAS Ctlgrs151341193
StatusMerged into rs151341192
Max Magnitude0
ClinVar
Risk rs151341193(G;G)
Alt rs151341193(G;G)
Reference rs151341193(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324540T>C
CLNSRC
CLNACC