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rs151341137

From SNPedia

Merged intors151341136
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341137(C;C)
Make rs151341137(C;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356812
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341137
ebirs151341137
HLIrs151341137
Exacrs151341137
Varsomers151341137
Maprs151341137
PheGenIrs151341137
hapmaprs151341137
1000 genomesrs151341137
hgdprs151341137
ensemblrs151341137
gopubmedrs151341137
geneviewrs151341137
scholarrs151341137
googlers151341137
pharmgkbrs151341137
gwascentralrs151341137
openSNPrs151341137
23andMers151341137
23andMe allrs151341137
SNP Nexus

SNPshotrs151341137
SNPdbers151341137
MSV3drs151341137
GWAS Ctlgrs151341137
StatusMerged into rs151341136
Max Magnitude0
ClinVar
Risk rs151341137(C;C)
Alt rs151341137(C;C)
Reference rs151341137(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324589C>G
CLNSRC
CLNACC