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rs151341388

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341388(-;-)
Make rs151341388(-;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355317
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341388
ebirs151341388
HLIrs151341388
Exacrs151341388
Varsomers151341388
Maprs151341388
PheGenIrs151341388
hapmaprs151341388
1000 genomesrs151341388
hgdprs151341388
ensemblrs151341388
gopubmedrs151341388
geneviewrs151341388
scholarrs151341388
googlers151341388
pharmgkbrs151341388
gwascentralrs151341388
openSNPrs151341388
23andMers151341388
23andMe allrs151341388
SNP Nexus

SNPshotrs151341388
SNPdbers151341388
MSV3drs151341388
GWAS Ctlgrs151341388
Max Magnitude0
ClinVar
Risk rs151341388(;)
Alt rs151341388(;)
Reference rs151341388(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323094delC
CLNSRC
CLNACC