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rs151341224

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341224(C;T)
Make rs151341224(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356408
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341224
ebirs151341224
HLIrs151341224
Exacrs151341224
Varsomers151341224
Maprs151341224
PheGenIrs151341224
hapmaprs151341224
1000 genomesrs151341224
hgdprs151341224
ensemblrs151341224
gopubmedrs151341224
geneviewrs151341224
scholarrs151341224
googlers151341224
pharmgkbrs151341224
gwascentralrs151341224
openSNPrs151341224
23andMers151341224
23andMe allrs151341224
SNP Nexus

SNPshotrs151341224
SNPdbers151341224
MSV3drs151341224
GWAS Ctlgrs151341224
Max Magnitude0
ClinVar
Risk rs151341224(A,G,T;A,G,T)
Alt rs151341224(A,G,T;A,G,T)
Reference rs151341224(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324185G>A; NC_000006.11:g.31324185G>C; NC_000006.11:g.31324185G>T
CLNSRC
CLNACC