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rs151341381

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341381(-;-)
Make rs151341381(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323101
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341381
dbSNP (classic)rs151341381
ClinGenrs151341381
ebirs151341381
HLIrs151341381
Exacrs151341381
Gnomadrs151341381
Varsomers151341381
LitVarrs151341381
Maprs151341381
PheGenIrs151341381
Biobankrs151341381
1000 genomesrs151341381
hgdprs151341381
ensemblrs151341381
geneviewrs151341381
scholarrs151341381
googlers151341381
pharmgkbrs151341381
gwascentralrs151341381
openSNPrs151341381
23andMers151341381
SNPshotrs151341381
SNPdbers151341381
MSV3drs151341381
GWAS Ctlgrs151341381
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341381(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323101delC
CLNSRC
CLNACC