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rs151341337

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341337(-;-)
Make rs151341337(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355855
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341337
ebirs151341337
HLIrs151341337
Exacrs151341337
Varsomers151341337
Maprs151341337
PheGenIrs151341337
hapmaprs151341337
1000 genomesrs151341337
hgdprs151341337
ensemblrs151341337
gopubmedrs151341337
geneviewrs151341337
scholarrs151341337
googlers151341337
pharmgkbrs151341337
gwascentralrs151341337
openSNPrs151341337
23andMers151341337
23andMe allrs151341337
SNP Nexus

SNPshotrs151341337
SNPdbers151341337
MSV3drs151341337
GWAS Ctlgrs151341337
Max Magnitude0
ClinVar
Risk rs151341337(;)
Alt rs151341337(;)
Reference rs151341337(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323632delC
CLNSRC
CLNACC