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rs151341222

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341222(C;T)
Make rs151341222(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356411
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341222
ebirs151341222
HLIrs151341222
Exacrs151341222
Varsomers151341222
Maprs151341222
PheGenIrs151341222
hapmaprs151341222
1000 genomesrs151341222
hgdprs151341222
ensemblrs151341222
gopubmedrs151341222
geneviewrs151341222
scholarrs151341222
googlers151341222
pharmgkbrs151341222
gwascentralrs151341222
openSNPrs151341222
23andMers151341222
23andMe allrs151341222
SNP Nexus

SNPshotrs151341222
SNPdbers151341222
MSV3drs151341222
GWAS Ctlgrs151341222
Max Magnitude0
ClinVar
Risk rs151341222(A,T;A,T)
Alt rs151341222(A,T;A,T)
Reference rs151341222(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324188G>A; NC_000006.11:g.31324188G>T
CLNSRC
CLNACC