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rs151341208

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341208(C;G)
Make rs151341208(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356695
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341208
ebirs151341208
HLIrs151341208
Exacrs151341208
Varsomers151341208
Maprs151341208
PheGenIrs151341208
hapmaprs151341208
1000 genomesrs151341208
hgdprs151341208
ensemblrs151341208
gopubmedrs151341208
geneviewrs151341208
scholarrs151341208
googlers151341208
pharmgkbrs151341208
gwascentralrs151341208
openSNPrs151341208
23andMers151341208
23andMe allrs151341208
SNP Nexus

SNPshotrs151341208
SNPdbers151341208
MSV3drs151341208
GWAS Ctlgrs151341208
Max Magnitude0
ClinVar
Risk rs151341208(G;G)
Alt rs151341208(G;G)
Reference rs151341208(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324472G>C
CLNSRC
CLNACC