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

rs151341318

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341318(C;C)
Make rs151341318(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356224
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341318
ebirs151341318
HLIrs151341318
Exacrs151341318
Varsomers151341318
Maprs151341318
PheGenIrs151341318
hapmaprs151341318
1000 genomesrs151341318
hgdprs151341318
ensemblrs151341318
gopubmedrs151341318
geneviewrs151341318
scholarrs151341318
googlers151341318
pharmgkbrs151341318
gwascentralrs151341318
openSNPrs151341318
23andMers151341318
23andMe allrs151341318
SNP Nexus

SNPshotrs151341318
SNPdbers151341318
MSV3drs151341318
GWAS Ctlgrs151341318
Max Magnitude0
ClinVar
Risk rs151341318(C;C)
Alt rs151341318(C;C)
Reference rs151341318(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31324001A>G
CLNSRC
CLNACC