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rs151341177

From SNPedia

Merged intors1065386
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341177(C;G)
Make rs151341177(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356770
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341177
ebirs151341177
HLIrs151341177
Exacrs151341177
Varsomers151341177
Maprs151341177
PheGenIrs151341177
hapmaprs151341177
1000 genomesrs151341177
hgdprs151341177
ensemblrs151341177
gopubmedrs151341177
geneviewrs151341177
scholarrs151341177
googlers151341177
pharmgkbrs151341177
gwascentralrs151341177
openSNPrs151341177
23andMers151341177
23andMe allrs151341177
SNP Nexus

SNPshotrs151341177
SNPdbers151341177
MSV3drs151341177
GWAS Ctlgrs151341177
StatusMerged into rs1065386
Max Magnitude0
ClinVar
Risk rs151341177(A,G;A,G)
Alt rs151341177(A,G;A,G)
Reference rs151341177(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324547G>T
CLNSRC
CLNACC