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rs151341261

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341261(-;-)
Make rs151341261(-;C)
ReferenceGRCh37.p5 37.3/137
Chromosome6
Position31324070
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341261
ebirs151341261
HLIrs151341261
Exacrs151341261
Varsomers151341261
Maprs151341261
PheGenIrs151341261
hapmaprs151341261
1000 genomesrs151341261
hgdprs151341261
ensemblrs151341261
gopubmedrs151341261
geneviewrs151341261
scholarrs151341261
googlers151341261
pharmgkbrs151341261
gwascentralrs151341261
openSNPrs151341261
23andMers151341261
23andMe allrs151341261
SNP Nexus

SNPshotrs151341261
SNPdbers151341261
MSV3drs151341261
GWAS Ctlgrs151341261
StatusDeleted
Max Magnitude0
ClinVar
Risk rs151341261(;)
Alt rs151341261(;)
Reference rs151341261(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324070delG
CLNSRC
CLNACC