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rs151341092

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341092(G;G)
Make rs151341092(G;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356937
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341092
ebirs151341092
HLIrs151341092
Exacrs151341092
Varsomers151341092
Maprs151341092
PheGenIrs151341092
hapmaprs151341092
1000 genomesrs151341092
hgdprs151341092
ensemblrs151341092
gopubmedrs151341092
geneviewrs151341092
scholarrs151341092
googlers151341092
pharmgkbrs151341092
gwascentralrs151341092
openSNPrs151341092
23andMers151341092
23andMe allrs151341092
SNP Nexus

SNPshotrs151341092
SNPdbers151341092
MSV3drs151341092
GWAS Ctlgrs151341092
Max Magnitude0
ClinVar
Risk rs151341092(G;G)
Alt rs151341092(G;G)
Reference rs151341092(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324714A>C
CLNSRC
CLNACC