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rs151341126

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341126(-;-)
Make rs151341126(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324594
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341126
ebirs151341126
HLIrs151341126
Exacrs151341126
Varsomers151341126
Maprs151341126
PheGenIrs151341126
hapmaprs151341126
1000 genomesrs151341126
hgdprs151341126
ensemblrs151341126
gopubmedrs151341126
geneviewrs151341126
scholarrs151341126
googlers151341126
pharmgkbrs151341126
gwascentralrs151341126
openSNPrs151341126
23andMers151341126
23andMe allrs151341126
SNP Nexus

SNPshotrs151341126
SNPdbers151341126
MSV3drs151341126
GWAS Ctlgrs151341126
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341126(;)
Alt rs151341126(;)
Reference rs151341126(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324594delG
CLNSRC
CLNACC