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rs144012689

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs144012689(A;A)
Make rs144012689(A;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position31355003
GeneHLA-B
is asnp
is mentioned by
dbSNPrs144012689
ebirs144012689
HLIrs144012689
Exacrs144012689
Varsomers144012689
Maprs144012689
PheGenIrs144012689
hapmaprs144012689
1000 genomesrs144012689
hgdprs144012689
ensemblrs144012689
gopubmedrs144012689
geneviewrs144012689
scholarrs144012689
googlers144012689
pharmgkbrs144012689
gwascentralrs144012689
openSNPrs144012689
23andMers144012689
23andMe allrs144012689
SNP Nexus

SNPshotrs144012689
SNPdbers144012689
MSV3drs144012689
GWAS Ctlgrs144012689
GMAF0.00551
Max Magnitude0
ClinVar
Risk rs144012689(A;A)
Alt rs144012689(A;A)
Reference rs144012689(T;T)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31322780T>A
CLNSRC
CLNACC