rs398122842
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GGGGGGG;GGGGGGG) | 0 | common in clinvar |
Make rs398122842(-;-) |
Make rs398122842(-;GGGGGGG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 19 |
Position | 48955715 |
Gene | BAX |
is a | snp |
is | mentioned by |
dbSNP | rs398122842 |
dbSNP (classic) | rs398122842 |
ClinGen | rs398122842 |
ebi | rs398122842 |
HLI | rs398122842 |
Exac | rs398122842 |
Gnomad | rs398122842 |
Varsome | rs398122842 |
LitVar | rs398122842 |
Map | rs398122842 |
PheGenI | rs398122842 |
Biobank | rs398122842 |
1000 genomes | rs398122842 |
hgdp | rs398122842 |
ensembl | rs398122842 |
geneview | rs398122842 |
scholar | rs398122842 |
rs398122842 | |
pharmgkb | rs398122842 |
gwascentral | rs398122842 |
openSNP | rs398122842 |
23andMe | rs398122842 |
SNPshot | rs398122842 |
SNPdbe | rs398122842 |
MSV3d | rs398122842 |
GWAS Ctlg | rs398122842 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs398122842(-;-) |
Alt | rs398122842(-;-) |
Reference | Rs398122842(GGGGGGG;GGGGGGG) |
Significance | Pathogenic |
Disease | T-cell acute lymphoblastic leukemia |
Variation | info |
Gene | BAX |
CLNDBN | T-cell acute lymphoblastic leukemia |
Reversed | 0 |
HGVS | NC_000019.9:g.49458972_49458978delGGGGGGG |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000010122.5, |