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rs151341094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341094(A;A)
Make rs151341094(A;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356929
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341094
ebirs151341094
HLIrs151341094
Exacrs151341094
Varsomers151341094
Maprs151341094
PheGenIrs151341094
hapmaprs151341094
1000 genomesrs151341094
hgdprs151341094
ensemblrs151341094
gopubmedrs151341094
geneviewrs151341094
scholarrs151341094
googlers151341094
pharmgkbrs151341094
gwascentralrs151341094
openSNPrs151341094
23andMers151341094
23andMe allrs151341094
SNP Nexus

SNPshotrs151341094
SNPdbers151341094
MSV3drs151341094
GWAS Ctlgrs151341094
Max Magnitude0
ClinVar
Risk rs151341094(A,T;A,T)
Alt rs151341094(A,T;A,T)
Reference rs151341094(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324706G>T
CLNSRC
CLNACC