Have questions? Visit https://www.reddit.com/r/SNPedia

rs151341070

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs151341070(-;-)
Make rs151341070(-;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31357309
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341070
ebirs151341070
HLIrs151341070
Exacrs151341070
Varsomers151341070
Maprs151341070
PheGenIrs151341070
hapmaprs151341070
1000 genomesrs151341070
hgdprs151341070
ensemblrs151341070
gopubmedrs151341070
geneviewrs151341070
scholarrs151341070
googlers151341070
pharmgkbrs151341070
gwascentralrs151341070
openSNPrs151341070
23andMers151341070
23andMe allrs151341070
SNP Nexus

SNPshotrs151341070
SNPdbers151341070
MSV3drs151341070
GWAS Ctlgrs151341070
Max Magnitude0
ClinVar
Risk rs151341070(;)
Alt rs151341070(;)
Reference rs151341070(C;C)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31325086delG
CLNSRC
CLNACC