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rs151341138

From SNPedia

Merged intors151341136
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341138(G;T)
Make rs151341138(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356812
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341138
ebirs151341138
HLIrs151341138
Exacrs151341138
Varsomers151341138
Maprs151341138
PheGenIrs151341138
hapmaprs151341138
1000 genomesrs151341138
hgdprs151341138
ensemblrs151341138
gopubmedrs151341138
geneviewrs151341138
scholarrs151341138
googlers151341138
pharmgkbrs151341138
gwascentralrs151341138
openSNPrs151341138
23andMers151341138
23andMe allrs151341138
SNP Nexus

SNPshotrs151341138
SNPdbers151341138
MSV3drs151341138
GWAS Ctlgrs151341138
StatusMerged into rs151341136
Max Magnitude0
ClinVar
Risk rs151341138(T;T)
Alt rs151341138(T;T)
Reference rs151341138(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324589C>A
CLNSRC
CLNACC