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rs151341129

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341129(-;-)
Make rs151341129(-;G)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324593
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341129
ebirs151341129
HLIrs151341129
Exacrs151341129
Varsomers151341129
Maprs151341129
PheGenIrs151341129
hapmaprs151341129
1000 genomesrs151341129
hgdprs151341129
ensemblrs151341129
gopubmedrs151341129
geneviewrs151341129
scholarrs151341129
googlers151341129
pharmgkbrs151341129
gwascentralrs151341129
openSNPrs151341129
23andMers151341129
23andMe allrs151341129
SNP Nexus

SNPshotrs151341129
SNPdbers151341129
MSV3drs151341129
GWAS Ctlgrs151341129
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341129(;)
Alt rs151341129(;)
Reference rs151341129(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324593delC
CLNSRC
CLNACC