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rs151341377

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341377(-;-)
Make rs151341377(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31323105
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341377
ebirs151341377
HLIrs151341377
Exacrs151341377
Varsomers151341377
Maprs151341377
PheGenIrs151341377
hapmaprs151341377
1000 genomesrs151341377
hgdprs151341377
ensemblrs151341377
gopubmedrs151341377
geneviewrs151341377
scholarrs151341377
googlers151341377
pharmgkbrs151341377
gwascentralrs151341377
openSNPrs151341377
23andMers151341377
23andMe allrs151341377
SNP Nexus

SNPshotrs151341377
SNPdbers151341377
MSV3drs151341377
GWAS Ctlgrs151341377
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341377(;)
Alt rs151341377(;)
Reference rs151341377(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31323105delG
CLNSRC
CLNACC