rs144943009
From SNPedia
Merged into | rs4999718 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs144943009(A;G) |
Make rs144943009(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 31356596 |
Gene | HLA-B |
is a | snp |
is | mentioned by |
dbSNP | rs144943009 |
dbSNP (classic) | rs144943009 |
ClinGen | rs144943009 |
ebi | rs144943009 |
HLI | rs144943009 |
Exac | rs144943009 |
Gnomad | rs144943009 |
Varsome | rs144943009 |
LitVar | rs144943009 |
Map | rs144943009 |
PheGenI | rs144943009 |
Biobank | rs144943009 |
1000 genomes | rs144943009 |
hgdp | rs144943009 |
ensembl | rs144943009 |
geneview | rs144943009 |
scholar | rs144943009 |
rs144943009 | |
pharmgkb | rs144943009 |
gwascentral | rs144943009 |
openSNP | rs144943009 |
23andMe | rs144943009 |
SNPshot | rs144943009 |
SNPdbe | rs144943009 |
MSV3d | rs144943009 |
GWAS Ctlg | rs144943009 |
Status | Merged into rs4999718 |
Max Magnitude | 0 |
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 |