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rs151341334

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341334(C;G)
Make rs151341334(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356179
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341334
ebirs151341334
HLIrs151341334
Exacrs151341334
Varsomers151341334
Maprs151341334
PheGenIrs151341334
hapmaprs151341334
1000 genomesrs151341334
hgdprs151341334
ensemblrs151341334
gopubmedrs151341334
geneviewrs151341334
scholarrs151341334
googlers151341334
pharmgkbrs151341334
gwascentralrs151341334
openSNPrs151341334
23andMers151341334
23andMe allrs151341334
SNP Nexus

SNPshotrs151341334
SNPdbers151341334
MSV3drs151341334
GWAS Ctlgrs151341334
Max Magnitude0
ClinVar
Risk rs151341334(G;G)
Alt rs151341334(G;G)
Reference rs151341334(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323956G>C
CLNSRC
CLNACC