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rs151341131

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341131(-;-)
Make rs151341131(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324590
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341131
dbSNP (classic)rs151341131
ClinGenrs151341131
ebirs151341131
HLIrs151341131
Exacrs151341131
Gnomadrs151341131
Varsomers151341131
LitVarrs151341131
Maprs151341131
PheGenIrs151341131
Biobankrs151341131
1000 genomesrs151341131
hgdprs151341131
ensemblrs151341131
geneviewrs151341131
scholarrs151341131
googlers151341131
pharmgkbrs151341131
gwascentralrs151341131
openSNPrs151341131
23andMers151341131
SNPshotrs151341131
SNPdbers151341131
MSV3drs151341131
GWAS Ctlgrs151341131
StatusDeleted
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs151341131(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324590delG
CLNSRC
CLNACC