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rs151341079

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341079(-;-)
Make rs151341079(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324759
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341079
dbSNP (classic)rs151341079
ClinGenrs151341079
ebirs151341079
HLIrs151341079
Exacrs151341079
Gnomadrs151341079
Varsomers151341079
LitVarrs151341079
Maprs151341079
PheGenIrs151341079
Biobankrs151341079
1000 genomesrs151341079
hgdprs151341079
ensemblrs151341079
geneviewrs151341079
scholarrs151341079
googlers151341079
pharmgkbrs151341079
gwascentralrs151341079
openSNPrs151341079
23andMers151341079
SNPshotrs151341079
SNPdbers151341079
MSV3drs151341079
GWAS Ctlgrs151341079
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341079(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324759delC
CLNSRC
CLNACC