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rs144943009

From SNPedia

Merged intors4999718
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs144943009(A;G)
Make rs144943009(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position31356596
GeneHLA-B
is asnp
is mentioned by
dbSNPrs144943009
ebirs144943009
HLIrs144943009
Exacrs144943009
Varsomers144943009
Maprs144943009
PheGenIrs144943009
hapmaprs144943009
1000 genomesrs144943009
hgdprs144943009
ensemblrs144943009
gopubmedrs144943009
geneviewrs144943009
scholarrs144943009
googlers144943009
pharmgkbrs144943009
gwascentralrs144943009
openSNPrs144943009
23andMers144943009
23andMe allrs144943009
SNP Nexus

SNPshotrs144943009
SNPdbers144943009
MSV3drs144943009
GWAS Ctlgrs144943009
StatusMerged into rs4999718
Max Magnitude0
ClinVar
Risk rs144943009(G;G)
Alt rs144943009(G;G)
Reference rs144943009(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-B
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31324373A>G
CLNSRC
CLNACC