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rs151341152

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341152(C;C)
Make rs151341152(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356804
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341152
ebirs151341152
HLIrs151341152
Exacrs151341152
Varsomers151341152
Maprs151341152
PheGenIrs151341152
hapmaprs151341152
1000 genomesrs151341152
hgdprs151341152
ensemblrs151341152
gopubmedrs151341152
geneviewrs151341152
scholarrs151341152
googlers151341152
pharmgkbrs151341152
gwascentralrs151341152
openSNPrs151341152
23andMers151341152
23andMe allrs151341152
SNP Nexus

SNPshotrs151341152
SNPdbers151341152
MSV3drs151341152
GWAS Ctlgrs151341152
Merged fromRs151341153
Max Magnitude0
ClinVar
Risk rs151341152(C,G;C,G)
Alt rs151341152(C,G;C,G)
Reference rs151341152(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324581A>C; NC_000006.11:g.31324581A>G
CLNSRC
CLNACC