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rs151341149

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs151341149(-;-)
Make rs151341149(-;A)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324582
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341149
dbSNP (classic)rs151341149
ClinGenrs151341149
ebirs151341149
HLIrs151341149
Exacrs151341149
Gnomadrs151341149
Varsomers151341149
LitVarrs151341149
Maprs151341149
PheGenIrs151341149
Biobankrs151341149
1000 genomesrs151341149
hgdprs151341149
ensemblrs151341149
geneviewrs151341149
scholarrs151341149
googlers151341149
pharmgkbrs151341149
gwascentralrs151341149
openSNPrs151341149
23andMers151341149
SNPshotrs151341149
SNPdbers151341149
MSV3drs151341149
GWAS Ctlgrs151341149
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341149(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324582delT
CLNSRC
CLNACC