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

rs151341091

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151341091(A;A)
Make rs151341091(A;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356941
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341091
ebirs151341091
HLIrs151341091
Exacrs151341091
Varsomers151341091
Maprs151341091
PheGenIrs151341091
hapmaprs151341091
1000 genomesrs151341091
hgdprs151341091
ensemblrs151341091
gopubmedrs151341091
geneviewrs151341091
scholarrs151341091
googlers151341091
pharmgkbrs151341091
gwascentralrs151341091
openSNPrs151341091
23andMers151341091
23andMe allrs151341091
SNP Nexus

SNPshotrs151341091
SNPdbers151341091
MSV3drs151341091
GWAS Ctlgrs151341091
Max Magnitude0
ClinVar
Risk rs151341091(A,C;A,C)
Alt rs151341091(A,C;A,C)
Reference rs151341091(G;G)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324718C>G; NC_000006.11:g.31324718C>T
CLNSRC
CLNACC