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

rs151341421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs151341421(C;C)
Make rs151341421(C;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31354360
GeneHLA-B
is asnp
is mentioned by
dbSNPrs151341421
dbSNP (classic)rs151341421
ClinGenrs151341421
ebirs151341421
HLIrs151341421
Exacrs151341421
Gnomadrs151341421
Varsomers151341421
LitVarrs151341421
Maprs151341421
PheGenIrs151341421
Biobankrs151341421
1000 genomesrs151341421
hgdprs151341421
ensemblrs151341421
geneviewrs151341421
scholarrs151341421
googlers151341421
pharmgkbrs151341421
gwascentralrs151341421
openSNPrs151341421
23andMers151341421
SNPshotrs151341421
SNPdbers151341421
MSV3drs151341421
GWAS Ctlgrs151341421
Max Magnitude0
ClinVar
Risk rs151341421(C;C)
Alt rs151341421(C;C)
Reference Rs151341421(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31322137A>G
CLNSRC
CLNACC